Category: thiazole

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.3034-53-5,2-Bromothiazole,as a common compound, the synthetic route is as follows.

General procedure: Substrate (0.1 mmol) and catalyst (2 mol%, 2 mumol) were mixed in 3 cm3 THF, organozinc reagent (1.3 mmol), and LiCl (1.3 mmol) were added at room temperature. After 6 h at 60 C, the solution was allowed to reach room temperature. NaCl solution (15%, 1 cm3) was added carefully, the organic layer was dried over MgSO4, evaporated and purified via silica column chromatography.

3034-53-5, The synthetic route of 3034-53-5 has been constantly updated, and we look forward to future research findings.

Reference：
Article; Mastalir, Mathias; Kirchner, Karl; Monatshefte fur Chemie; vol. 148; 1; (2017); p. 105 – 109;,
Thiazole | C3H3NS – PubChem
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With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.15864-32-1,2-Amino-6-bromobenzothiazole,as a common compound, the synthetic route is as follows.

Example 1 (Method A); N-(6-(2-(3-(pyridin-3-yl)propoxy)pyrimidin-4-yl)benzo[d]thiazol-2-yl)acetamide; Step 1. N-(6-bromobenzopd’|thiazol-2-yl)acetamide; 6-Bromobenzo[d]thiazol-2-amine (Aldrich, St. Louis, MO; 10.02 g, 43.7 mmol) was suspended in DCM (175 mL) to which DMAP (6.107 g, 50.0 mmol) was added. The flask was cooled in an ice water bath under argon, and acetic anhydride (4.60 mL, 48.8 mmol) was added, and the reaction was warmed to RT and stirred overnight. The reaction was washed with 10% HCl and water. The precipitate in the organic phase was filtered. The aqueous washings were extracted with DCM and 10: 1 DCM / MeOH. These extracts were concentrated, combined with the filtrate from the above filtration, and concentrated again. The solid was collected (from the filtration as well as the aqueous workup), concentrated, and dried under vacuum to afford the desired N-(6-bromobenzo[d]thiazol-2-yl) acetamide (12.30 g, 45.39 mmol, 88% purity, 91% yield). MS (ESI pos. ion) m/z: 271 (MH+, 79Br), 273 (MH+, 81Br). Calculated exact mass for C9H7BrN2OS: 270 (79Br), 272 (81Br)., 15864-32-1

The synthetic route of 15864-32-1 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; AMGEN INC.; WO2009/17822; (2009); A2;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.939-69-5,6-Hydroxybenzo[d]thiazole-2-carbonitrile,as a common compound, the synthetic route is as follows.,939-69-5

General procedure: The hydroxy- or methoxycarbonitrile derivative (1 eq) was added to the cysteine derivative (1.05 eq) and sodium carbonate (3 eq) in 5 ml water. The mixture was stirred at room temperature for three hours before addition of dilute HCl (1 M) to pH ? 3.5 ? 4.0. The product was isolated by extraction with diethyl ether, washed by water, followed by evaporation

939-69-5 6-Hydroxybenzo[d]thiazole-2-carbonitrile 9881912, athiazole compound, is more and more widely used in various fields.

Reference：
Article; Rothweiler, Ulli; Eriksson, Jonas; Stensen, Wenche; Leeson, Frederick; Engh, Richard A.; Svendsen, John S.; European Journal of Medicinal Chemistry; vol. 94; (2015); p. 140 – 148;,
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133692-16-7, 2-Amino-5-bromo-4-methylthiazole hydrochloride is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

EXAMPLE 64 A mixture of 2-amino-5-bromo-4-methylthiazole hydrochloride (1.15 g), 2-mercaptopyrimidine (0.6 g) and potassium carbonate (1.7 g) in N,N-dimethylformamide (20 ml) was heated at 90 C. for 3.5 hours with stirring. The reaction mixture was poured into ice water. The mixture was extracted with a mixture of tetrahydrofuran and ethyl acetate (1:1), washed with aqueous saturated sodium chloride and dried over magnesium sulfate. The solvent was concentrated under reduced pressure to give solid. The solid was subjected to column chromatography on silica gel (silica gel 60, 70-230 mesh,; Merck: 100 g) and eluted with a mixture of chloroform and methanol (10:1). The fractions containing the objective compound were combined and concentrated under reduced pressure to give 2-amino-4-methyl-5-(2-pyrimidinylthio)thiazole (0.65 g, yield: 58.0%). mp: 165-170 C. (dec.) IR (Nujol): 3300, 3175, 1630, 1555, 1490, 1320 cm-1 NMR (DMSO-d6, 200 MHZ, ppm): 2.10 (3H, s), 7.24-7.33 (1H, m), 7.33 (2H, s), 8.64 (2H, d, J=5Hz) Mass: M+1 225, M 224, m/e 209, 191, 182, 166, 145, 133692-16-7

As the paragraph descriping shows that 133692-16-7 is playing an increasingly important role.

Reference：
Patent; Fujisawa Pharmaceutical Co., Ltd.; US5256675; (1993); A;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

3622-35-3, Benzo[d]thiazole-6-carboxylic acid is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

3622-35-3, Methyl benzothiazole-6-carboxylate S2b[0131] A 0.2 M stirring solution of benzothiazole-6-carboxylic acid in THF (17 mL) was cooled to 0 0C. Excess diazomethane was introduced in situ from Diazald (2.51 g, 11.7 mmol), according to literature procedure. Lombardi, P. Chem. Ind. (London) 1990, 708. After addition of the diazomethane, the solution was stirred at 0 0C for 30 min and then at room temperature for 30 min. The solvent was removed under reduced pressure to afford 0.621 g (96%) of S2b as a tan solid, mp 105-106 0C. 1H NMR (400 MHz, CDCl3): delta 3.95 (s, 3H), 8.13-8.18 (m, 2H), 4), 7.93 (dd, IH, J= 0.8, 1.2), 9.14 (s, IH). 13C-NMR (100 MHz, CDCl3): delta 52.6, 123.6, 124.4, 127.5, 127.6, 133.9, 156.2, 157.5, 166.7. HRMS-FAB (m/z): [MH]+ calcd for C9H8NO2S, 194.0276; found, 194.0270.

As the paragraph descriping shows that 3622-35-3 is playing an increasingly important role.

Reference：
Patent; THE REGENTS OF THE UNIVERSITY OF CALIFORNIA; WO2009/75778; (2009); A2;,
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Thiazole | chemical compound | Britannica

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.15448-99-4,2-Methylbenzo[d]isothiazol-3(2H)-one 1,1-dioxide,as a common compound, the synthetic route is as follows.

15448-99-4, B. 2-methoxyethyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide To a solution of 3.0 g. (0.015 mole) of N-methylsaccharin and 2.3 g. (0.015 mole) of 2-methoxyethyl chloroacetate in 15 ml. of dimethylsulfoxide at 40 C. was added 810 mg. (0.033 mole) of sodium hydride over a 2 hour period. The resulting reaction mixture was stirred for 2 hours at 40-50 C. and was then quenched in 5% hydrochloric acid solution. The resulting suspension was extracted with methylene chloride (2*100 ml.) and the organic layers separated, combined and washed with water (50 ml.) and a brine solution (50 ml). The organic layer was dried over magnesium sulfate and concentrated to an oil, 4.1 g. The product was purified by dissolution of the residue in 5 ml. of acetone and addition of the acetone slowly to 125 ml. of 0.25N hydrochloric acid. The suspension was allowed to stir for several hours, and was then filtered and dried 2.6 g. (55%). The product is indistinguishable from that reported in U.S. patent application Ser. No. 191,716, filed Sept. 29, 1980.

The synthetic route of 15448-99-4 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; Pfizer Inc.; US4483982; (1984); A;,
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Thiazole | chemical compound | Britannica

40283-41-8, 2-Aminothiazole-4-carboxylic acid is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

2-Aminothiazole-4~carboxylic acid (1A) (0.5 g, 3.47 mmol) and 4-(3-Amino- pyhdin~4-yl)-piperazine-1-carboxylic acid tert-butyl ester (1B) (Ig5 3.59) were combined with anhydrous dmethylformamide (15 mL) and N, N-diisopropylethylamine (1 mL, 5.5 mmol), before adding N-[(dimethylamino)-1H-1 .2l3-triazolo[4.5-jb]pyridine- 1 -yImethyfene]-A/-methylmethanaminium Hexaffuorophosphate N-oxle (HATU) (2 g, (5.3 mmol). The reaction was stirred at room temperature for 16 hours, then stripped of solvent and stirred with a mixture (25:75 v/v) of 1 M aqueous KOH and saturated aqueous NaHCtheta3. The sticky brown residue was filtered, then rinsed with acetone to provide compound 1C (700 mg, 1.73 mmol, 50%) as an off-white solid. HPLC-MS tR ~ 1.076 min (UV 254). Mass calculated for formula C18H24N6O3S 404.49; observed IvIH+ (LCMS) 405.1 (m/z).

40283-41-8, The synthetic route of 40283-41-8 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; SCHERING CORPORATION; WO2009/58739; (2009); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

64987-16-2, Methyl 2-(2-aminothiazol-4-yl)acetate is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

Boc-anhydride (1 .53 mL, 6.6 mmol) was added to methyl 2-(2-aminothiazol-4-yl)acetate (1 .08 g, 6.28 mmol), N,N-diisopropylethylamine (1 .21 mL, 6.91 mmol) and DMAP (8 mg, 0.06 mmol) in THF (20 mL) at 0 C. The reaction mixture was warmed to room temperature and stirred overnight, then heated to 90 C. After 2 h the reaction was concentrated, and the residue was purified on silica gel, eluting with a 0%-100% EtOAc-hexanes gradient to give the title compound (1 .35 g, 79%). 1H NMR (400 MHz, CD3SOCD3) delta 1 .44 (s, 9 H), 1 .96 (s, 2 H), 3.62 (s, 3 H), 6.89 (s, 1 H), 1 1 .39 (s, 1 H); LC-MS (LC-ES) M-H = 271 ., 64987-16-2

The synthetic route of 64987-16-2 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED; DEATON, David Norman; GUO, Yu; HANCOCK, Ashley Paul; SCHULTE, Christie; SHEARER, Barry George; SMITH, Emilie Despagnet; STEWART, Eugene L.; THOMSON, Stephen Andrew; (556 pag.)WO2018/69863; (2018); A1;,
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3034-53-5, 2-Bromothiazole is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

The (4-formylphenyl)boronic acid 118 (0.30 g, 2.0 mmol), 2-bromo-1,3-thiazole 119a (0.33 g, 2.0 mmol), Pd(PPh3)4(0.12 g, 0.1 mmol), aqueous solution of potassium carbonate (0.4 M, 5 mL), ethanol (5 mL) and toluene (2 mL) were added to a 50 mL flask under nitrogen. The reaction mixture was stirred at 115 C. for 24 hours and then cooled to room temperature. After removing the solvent, the crude residue was purified by column chromatography on silica gel using EA/ hexane (1/5) as eluent. The product 120a was obtained as a white solid at a yield of 95%

3034-53-5, The synthetic route of 3034-53-5 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; National Health Research Institutes; Academia Sinica; Chen, Chih-Hao; Shih, Chuan; Chen, Chiung-Tong; Wang, Hwei-Jiung; Huang, Kai-Fa; US2020/71312; (2020); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

3622-35-3, Benzo[d]thiazole-6-carboxylic acid is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

STEP A: Preparation of benzothiazole-6-carboxylic acid (4-hydroxy-butyl)-amide (14A). 2.69 g (15 mmol) of benzothiazole-6-carboxylic acid is dissolved in a mixture of l.34 g (15 mmol) 4-amino-butan-l-ol and 70 mL dry tetrahydrofuran. 2.43 g (15 mmol) of CDI is added after stirring for 30 minutes and then stirred for another hour. The mixture is concentrated in vacuum. The resulting residue is suspended in dichloromethane, water is added, and the organic phase is separated. The aqueous phase is extracted with dichloromethane twice. The combined organic phases are dried over sodium sulfate and concentrated in vacuum. Yield: 55%; ESI-MS: 251 (M+H+)., 3622-35-3

3622-35-3 Benzo[d]thiazole-6-carboxylic acid 601670, athiazole compound, is more and more widely used in various fields.

Reference：
Patent; MOTAC NEUROSCIENCE LIMITED; WO2009/56805; (2009); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica