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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11601생성일: 2026년 10월 24일

Diisopropylethylamine → (S)-4-(5-chloroindole-2-carbonylamino)-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-one

https://huagongshe.com/ko/reaction/11601

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-Chloro-1H-indole-2-carboxylic acidHCID 82693—
반응물HOAtHCID 181649—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(S)-4-amino-1,2,4,5-tetrahydro-3H-benzo[c]azepin-3-one hydrochlorideHCID 69196954—
용매TetrahydrofuranHCID 8028—
생성물(S)-4-(5-chloroindole-2-carbonylamino)-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-oneHCID 9998223—

반응 단계

A mixture of (S)-4-amino-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-one hydrochloride (all of that prepared above), tetrahydrofuran (25 mL), 5-chloroindole-2-carboxylic acid (198 mg), 1-hydroxy-7-azabenzotriazole (150 mg), and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (210 mg) was stirred at room temperature. Diisopropylethylamine (202 mg) was added, and after 16 h the resulting yellow solution was evaporated under vacuum. The residue was dissolved in ethyl acetate (150 mL), and this was washed sequentially with 1.0 M aqueous hydrochloric acid (50 mL twice), 1.0 M aqueous sodium hydroxide (50 mL), water (50 mL), and brine (25 mL), dried over anhydrous sodium sulfate, and evaporated under vacuum to provide crude product. The product was crystallized by dissolving in warm methanol (40 mL) and adding diethyl ether (100 mL). The crystals were filtered, washed with diethyl ether (30 mL twice), and dried under vacuum to provide the title compound (181 mg). HPLC/MS [M+H]+, 354.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098235B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-3f80ff37dc2a4555bcb5ef06034a0b77
출처 메모uspto-grants-2006_08