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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 5-Chloro-1H-indole-2-carboxylic acid | HCID 82693 | — |
| 반응물 | HOAt | HCID 181649 | — |
| 반응물 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 반응물 | (S)-4-amino-1,2,4,5-tetrahydro-3H-benzo[c]azepin-3-one hydrochloride | HCID 69196954 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (S)-4-(5-chloroindole-2-carbonylamino)-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07098235B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-3f80ff37dc2a4555bcb5ef06034a0b77 |
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| 출처 메모 | uspto-grants-2006_08 |
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