Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 348970생성일: 2026년 10월 25일
1-butyl-4-(1,3-oxazol-2-yl)-1H-indole-6-carboxylic acid → 1-Butyl-N-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-4-(1,3-oxazol-2-yl)-1H-indole-6-carboxamide
https://huagongshe.com/reaction/348970
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-butyl-4-(1,3-oxazol-2-yl)-1H-indole-6-carboxylic acid | HCID 21085169 | — |
| 반응물 | (2R,3S)-3-amino-4-(3,5-difluorophenyl)-1-[(3-ethylbenzyl)amino]butan-2-ol | HCID 57487282 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Butyl-N-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-4-(1,3-oxazol-2-yl)-1H-indole-6-carboxamide | HCID 57512965 | 23.3% |
반응 단계
To a mixture of 1-butyl-4-(1,3-oxazol-2-yl)-1H-indole-6-carboxylic acid (0.2 g) in methylene chloride (20 mL) was added 1,1-carbonyldiimidazole (0.114 g). The mixture was stirred at room temperature for 1 h at which time (2R,3S)-3-amino-4-(3,5-difluorophenyl)-1-[(3-ethylbenzyl)amino]butan-2-ol (0.265 g) dissolved in methylene chloride (10 mL) was added. The mixture was stirred at room temperature for 18 h then poured into methylene chloride (50 mL), washed with water followed by brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Column chromatography on silica gel (100 mL) using 65% methylene chloride, 30% hexanes, and 5% methanol as eluent to give 0.0985 g of the title compound: MS (ESI+) for C35H38F2N4O3 m/z 601.99 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07176242B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-10404e80df284cbdb3324993fe62bec9 |
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| 출처 메모 | uspto-grants-2007_02 |
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