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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84413생성일: 2026년 10월 24일

Triethylamine → N-(2-(tert-butyldimethylsilyloxy)ethyl)-N-(2-chlorophenyl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamide

https://huagongshe.com/ko/reaction/84413

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4,5-Dihydrobenzo[b]thieno[2,3-d]oxepine-2-carbonylchlorideHCID 57900147—
반응물N-(2-(tert-butyldimethylsilyloxy)ethyl)-2-chloroanilineHCID 66868760—
용매TetrahydrofuranHCID 8028—
생성물N-(2-(tert-butyldimethylsilyloxy)ethyl)-N-(2-chlorophenyl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamideHCID 5790015071.9%

반응 단계

To a solution of N-(2-(tert-butyldimethylsilyloxy)ethyl)-2-chloroaniline (0.145 g, 0.508 mmol) and triethylamine (0.113 mL, 0.812 mmol) in tetrahydrofuran (1 mL, 10 mmol) was added a solution of 4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carbonyl chloride (0.107 g, 0.406 mmol) in tetrahydrofuran (4 mL). The reaction was stirred overnight and concentrated in vacuo. Aqueous work up gave a yellow solid which was purified on silica by MPLC to give 150 mg of N-(2-(tert-butyldimethylsilyloxy)ethyl)-N-(2-chlorophenyl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846762B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c1ffed0b9a24450082243ac2aaa200cf
출처 메모uspto-grants-2014_09