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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73604생성일: 2026년 10월 24일

1,2-Dichloroethane → (S)-tert-butyl 1-(3-(2-bromothiazole-4-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamate

https://huagongshe.com/ko/reaction/73604

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물HOAtHCID 181649—
반응물2-Bromo-1,3-thiazole-4-carboxylic acidHCID 2763209—
반응물(S)-tert-Butyl (1-(3-aminopyridin-4-yl)piperidin-3-yl)carbamateHCID 59332360—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(S)-tert-butyl 1-(3-(2-bromothiazole-4-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamateHCID 58182192—

반응 단계

A solution containing 1 eq each of (S)-tert-butyl 1-(3-aminopyridin-4-yl)piperidin-3-ylcarbamate, 2-bromothiazole-4-carboxylic acid, HOAT and EDC in DMF, at a concentration of 0.5 M, was stirred for 60 hours. The solution was diluted with EtOAc and was washed with H2O (4×), NaCl(sat.), was dried over MgSO4, was filtered and the volatiles were removed in vacuo yielding (S)-tert-butyl 1-(3-(2-bromothiazole-4-carboxamido)pyridin-4-yl)piperidin-3-ylcarbamate, LCMS (m/z): 416.1 (MH+); LC Rt=1.95 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829193B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9cba713dadc948a0895d267fc4072871
출처 메모uspto-grants-2014_09