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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 912676생성일: 2026년 10월 26일

Benzoyl isothiocyanate → tert-butyl 4-fluoro-3-[(6-oxo-2-thioxo-1,2,6,7-tetrahydro-3H-purin-3-yl)methyl]-1H-indole-1-carboxylate

https://huagongshe.com/reaction/912676

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl isothiocyanateHCID 68284—
반응물tert-butyl 3-({[5-(aminocarbonyl)-1H-imidazol-4-yl]amino}methyl)-4-fluoro-1H-indole-1-carboxylateHCID 67417268—
용매DichloromethaneHCID 6344—
생성물tert-butyl 4-fluoro-3-[(6-oxo-2-thioxo-1,2,6,7-tetrahydro-3H-purin-3-yl)methyl]-1H-indole-1-carboxylateHCID 8663112448%

반응 조건

온도80 °C

반응 단계

A solution of tert-butyl 3-({[5-(aminocarbonyl)-1H-imidazol-4-yl]amino}methyl)-4-fluoro-1H-indole-1-carboxylate (0.17 g, 0.45 mmol, obtained from Example 11(b)) and benzoyl isothiocyanate (0.073 mL, 0.54 mmol) in CH2Cl2 (5 mL) was stirred for 3 h 20 minutes and then evaporated. Ammonia (7 M in MeOH, 4 mL) was added to the residue and the mixture was heated to 80° C. for 2 h and then evaporated. Purification by flash chromatography using MeOH (2%) in CHCl3 gave the title compound (0.089 g, 48%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08026244B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-b2adcce52c3f4ef780e218c95ce6ba45
출처 메모uspto-grants-2011_09