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HRID 491571作成日:2026年10月26日

Pyridine → 4-(4-chlorophenyl)-N-(2-methylbenzothiazol-5-yl)cyclohexane-1-carboxamide

https://huagongshe.com/reaction/491571

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物5-Benzothiazolamine, 2-methyl-HCID 36229—
反応物Oxalyl chlorideHCID 65578—
反応物4-(4-Chlorophenyl)cyclohexane-1-carboxylic acidHCID 2735792—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物4-(4-chlorophenyl)-N-(2-methylbenzothiazol-5-yl)cyclohexane-1-carboxamideHCID 10407712101.2%

反応条件

温度45 °C

反応手順

A suspension of 4-(4-chlorophenyl)-cyclohexane-1-carboxylic acid (100 mg, 0.42 mmol) in DCM (10 ml) was treated with catalytic DMF and oxalyl chloride (110 ul, 1.26 mmol) at 0° C. and the mixture was then stirred at room temp. for 1 h and at 45° C. for 2 h. The solvent and excess oxalyl chloride was removed in vacuo and the residue resuspended in DCM (5 ml). To this was added pyridine (35 ul, 0.42 mmol) and 5-amino-2-methylbenzothiazole (63 mg, 0.38 mmol) and the reaction stirred at room temp. overnight. MeOH (1 ml) was added and the mixture was washed with sat. aq. sodium bicarbonate solution and brine then dried (MgSO4) and concentrated to give the title compound as an off-white solid (148 mg). 1H NMR (400 MHz, DMSO) δ (ppm): 8.37 (d, 1H), 7.96 (d, 1H), 7.63 (dd, 1H), 7.40 (d, 2H), 7.38 (d, 2H), 2.83 (s, 3H), 2.49-2.63 (m, 2H), 2.04 (m, 2H), 1.94 (m, 2H), 1.69 (m, 2H), 1.53 (m, 2H). MS(ES): MH+ 385/387, M−H+ 383/385.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531558B2
出典データセットuspto-grants-2009_05
ORD IDord-33710b17ac3a426daf7d3f18064a41b1
出典メモuspto-grants-2009_05