Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18748생성일: 2026년 10월 25일
4-Fluorobenzylamine → tert-butyl (3aR,7aS)-2-[(4-fluorophenyl)methylamino]-3a,4,5,6,7,7a-hexahydrobenzimidazole-1-carboxylate
https://huagongshe.com/reaction/18748
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Fluorobenzylamine | HCID 67326 | — |
| 반응물 | cis-3a,4,5,6,7,7a-Hexahydro-2-methylthio-benzimidazole-1-carboxylic Acid, Tert-Butyl Ester | HCID 86596330 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | tert-butyl (3aR,7aS)-2-[(4-fluorophenyl)methylamino]-3a,4,5,6,7,7a-hexahydrobenzimidazole-1-carboxylate | HCID 68569432 | 98.1% |
반응 단계
A mixture of intermediate 76 (200 mg, 0.0.740 mmol), 4-fluorobenzylamine (0.5 mL, 4.4 mmol) is heated at 100° C. (reaction block) overnight. The reaction mixture is cooled to RT. The reaction mixture is diluted with dichloromethane, washed with 0.1N HCl, and brine. The solvent is evaporated, and the residue triturated with EtOAc, and the insoluble material filtered to give 252 mg of the product 193. 1H NMR (CDCl3) δ 8.55 (s, 1 H), 7.55-7.35 (m, 2 H), 7.10-7.00 (m, 2 H), 5.10-4.90 (m, 2 H), 4.30-4.10 (m, 2 H), 2.70-2.55 (m, 1 H), 2.20-2.05 (m, 1 H), 1.80-1.05 (m, 15 H); MS: m/z 348 (M++1)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741493B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-55c3c36fc7e34f6d9b1a5a99f0ea5893 |
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| 출처 메모 | uspto-grants-2010_06 |
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