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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491572생성일: 2026년 10월 26일

Triethylamine → 4-(2-Fluorophenyl)-N-(2-methylbenzothiazol-5-yl)-1-piperazine carboxamide

https://huagongshe.com/reaction/491572

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물5-Benzothiazolamine, 2-methyl-HCID 36229—
반응물1-(2-Fluorophenyl)piperazineHCID 70529—
반응물TriphosgeneHCID 94429—
용매DichloromethaneHCID 6344—
생성물4-(2-Fluorophenyl)-N-(2-methylbenzothiazol-5-yl)-1-piperazine carboxamideHCID 1009056193.1%

반응 단계

To a stirred solution of 5-amino-2-methylbenzothiazole (100 mg, 0.61 mmol) and triethylamine (170 ul, 1.22 mmol) in DCM (5 ml) at 0° C. under an argon atmosphere was added triphosgene (60 mg, 0.2 mmol). The mixture was warmed to room temp. and stirred for 1 h. 4-(2-Fluorophenyl)piperazine (110 mg, 0.61 mmol) was added and the reaction was stirred at room temp. overnight. The solvent was removed in vacuo and the residue purified by chromatography eluting with a 0-100% EtOAc/petroleum ether gradient to give the title compound as a pale yellow solid (69 mg). 1H NMR (400 MHz, CDCl3) δ (ppm): 7.82 (d, 1H), 7.71 (d, 1H), 7.53 (dd, 1H), 6.92-7.10 (m, 4H), 6.65 (s, 1H), 3.69 (m, 2H), 3.13 (m, 2H), 2.81 (s, 3H). MS(ES): MH+ 371, M−H+ 369.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531558B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-157e463f7efb4d5b9ea527d9ddd05e0f
출처 메모uspto-grants-2009_05