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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 711571생성일: 2026년 10월 25일

tert-butyl N-(5-(tributylstannyl)-1,3-thiazol-2-yl)carbamate → tert-Butyl (5-(6-(((1R,2S)-2-((tert-butoxycarbonyl)amino)cyclohexyl)amino)-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-4-yl)-1,3-thiazol-2-yl)carbamate

https://huagongshe.com/reaction/711571

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(5-(tributylstannyl)-1,3-thiazol-2-yl)carbamateHCID 2763269—
반응물tert-Butyl (1S,2R)-2-(4-chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)cyclohexylcarbamateHCID 86654712—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물tert-Butyl (5-(6-(((1R,2S)-2-((tert-butoxycarbonyl)amino)cyclohexyl)amino)-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-4-yl)-1,3-thiazol-2-yl)carbamateHCID 8665474164.7%

반응 단계

A solution of tert-butyl (1S,2R)-2-(4-chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)cyclohexylcarbamate (50 mg, 0.091 mmol), tert-butyl 5-(tributylstannyl)thiazol-2-ylcarbamate (53.5 mg, 0.109 mmol), and tetrakis(triphenylphosphine)palladium(0) (105 mg, 0.091 mmol) in toluene (1 mL) was heated to 102° C. for 24 h. After removal of the solvent, the resulting crude material was reconstituted in MeOH/DMF (6.0 mL) and purified via preparative HPLC eluting with water (0.05% TFA) and ACN (70-75% gradient, 0.035% TFA). The collected fractions were stripped to dryness via rotary evaporation to yield the title compound (42 mg, 64%). [M+H] calc'd for C35H45FN6O7S, 713. found, 713.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181255B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-d1c2ff6a3b6e4f5b9e93a3bf974485a3
출처 메모uspto-grants-2015_11