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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536101생성일: 2026년 10월 24일

Triethylamine → 1-[(5-Fluoro-1H-indol-3-yl)methyl]-2-thioxo-1,2,3,5-tetrahydro-pyrrolo[3,2-d]pyrimidin-4-one

https://huagongshe.com/ko/reaction/536101

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzoyl isothiocyanateHCID 68284—
반응물5-fluoro-1H-indole-3-carbaldehydeHCID 259089—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물3-Amino-2-ethoxycarbonylpyrrole hydrochlorideHCID 16427091—
용매MethanolHCID 887—
생성물1-[(5-Fluoro-1H-indol-3-yl)methyl]-2-thioxo-1,2,3,5-tetrahydro-pyrrolo[3,2-d]pyrimidin-4-oneHCID 1170239821.4%

반응 단계

3-Amino-1H-pyrrole-2-carboxylic acid ethyl ester hydrochloride (0.10 g, 0.52 mmol) was dissolved in methanol (4 mL) and 5-fluoro-1H-indole-3-carboxaldehyde (0.10 g, 0.63 mmol), NaCNBH3 (0.033 g, 0.52 mmol) and Et3N (0.073 g, 0.52 mmol) were added. The resulting mixture was stirred at r.t. overnight. Additional NaCNBH3 (0.01 g) was added and the mixture was heated at 50° C. for 5 h. The reaction mixture was cooled to r.t. and concentrated in vacuo. The crude intermediate was dissolved in CH2Cl2 (3 mL) and methanol (1 mL). Benzoyl isothiocyanate (0.078 mL, 0.58 mmol) was added and after stirring at r.t. for 1 h the mixture was concentrated in vacuo. The residue was dissolved in ammonia (7N in methanol, 3 mL) and heated at 80° C. for 2 h. The solvent was removed in vacuo and after purification by preparative HPLC, the title compound (0.035 g, 21%) was obtained as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859568B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-a04e86668dd74bb18d635926ec5be031
출처 메모uspto-grants-2014_10