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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1018827생성일: 2026년 10월 27일

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → N-(5-Bromo-thiazol-2-yl)-3-cyclohexyl-2-(5,6-dichloro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionamide

https://huagongshe.com/reaction/1018827

반응식

참여 물질

역할이름HCID투입량
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물(S)-3-cyclohexyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamideHCID 9947513—
반응물5-Bromo-1,3-thiazol-2-amine--hydrogen chloride (1/1)HCID 22170392—
반응물(S)-3-cyclohexyl-2-(5,6-dichloro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acidHCID 69695408—
생성물N-(5-Bromo-thiazol-2-yl)-3-cyclohexyl-2-(5,6-dichloro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionamideHCID 1840221340%

반응 단계

This compound was prepared via BOP coupling of (S)-3-cyclohexyl-2-(5,6-dichloro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acid (prepared in Example 4, Step C; 248 mg; 0.70 mmol) and 2-amino-5-bromothiazole hydrochloride (154 mg; 0.89 mmol) in a manner similar to that used for the preparation of (S)-3-cyclohexyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamide (outlined in Example 1, Step B) to provide N-(5-Bromo-thiazol-2-yl)-3-cyclohexyl-2-(5,6-dichloro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionamide as a beige solid in 40% yield: EI-HRMS m/e calcd for C20H20BrCl2N3O2S (M+) 514.9837, found 514.9836.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06482951B2
출처 데이터셋uspto-grants-2002_11
ORD IDord-b3945481f3214f2f92e695b06dc289c2
출처 메모uspto-grants-2002_11