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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60266생성일: 2026년 10월 24일

Triethylamine → (S)-4-(4-(2-(pyrrolidin-2-yl)acetyl)piperazin-1-yl)-9H-diprido[2,3-b;4',3'-d]pyrrole-6-carbonitrile

https://huagongshe.com/ko/reaction/60266

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물(S)-2-(1-BOC-2-pyrrolidinyl)acetic acidHCID 688605—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-(piperazin-1-yl)-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-6-carbonitrileHCID 67257416—
용매DichloromethaneHCID 6344—
생성물(S)-4-(4-(2-(pyrrolidin-2-yl)acetyl)piperazin-1-yl)-9H-diprido[2,3-b;4',3'-d]pyrrole-6-carbonitrileHCID 53250548—

반응 단계

A mixture of 4-(piperazin-1-yl)-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carbonitrile (100 mg, 0.2 mmol), (S)-2-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)acetic acid (220 mg, 1.0 mmol), 1-hydroxybenzotriazole (50 mg, 0.4 mmol), (3-dimethylamino-propyl)-ethyl-carbodiimide hydrogen chloride (70 mg, 0.4 mmol), and triethylamine (0.1 mL, 0.7 mmol) in methylene chloride (2.5 mL) was stirred at ambient temperature overnight. The reaction mixture was diluted with methylene chloride (50 mL) and washed with saturated aqueous sodium bicarbonate solution (20 mL). The organic layer was separated, dried over sodium sulfate, filtered, concentrated in vacuo, and purified flash chromatography (silica, 4 g, ISCO, 0-70% ethyl acetate in heptane) to afford the title compound as a white foam, which was used in the next step without any further purification (140 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440976B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-b31be6760dfb40c4b15d92d1ee43ef56
출처 메모uspto-grants-2016_09