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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491571생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/491571

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물5-Benzothiazolamine, 2-methyl-HCID 36229—
반응물Oxalyl chlorideHCID 65578—
반응물4-(4-Chlorophenyl)cyclohexane-1-carboxylic acidHCID 2735792—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4-(4-chlorophenyl)-N-(2-methylbenzothiazol-5-yl)cyclohexane-1-carboxamideHCID 10407712101.2%

반응 조건

온도45 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531558B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-33710b17ac3a426daf7d3f18064a41b1
출처 메모uspto-grants-2009_05