Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872307생성일: 2026년 10월 27일
Methyl 2-aminopyridine-4-carboxylate → 2-[4-(1-Tert-butoxycarbonylamino-cyclobutyl)-phenyl]-3-phenyl-imidazo[1,2-a]pyridine-7-carboxylic acid methyl ester
https://huagongshe.com/reaction/872307
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl 2-aminopyridine-4-carboxylate | HCID 236984 | — |
| 반응물 | tert-Butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamate | HCID 86691038 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-[4-(1-Tert-butoxycarbonylamino-cyclobutyl)-phenyl]-3-phenyl-imidazo[1,2-a]pyridine-7-carboxylic acid methyl ester | HCID 66665614 | 47% |
반응 단계
A mixture of {1-[4-(2-bromo-2-phenyl-acetyl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester [Int-1-A] (4.40 g, 9.91 mmol), methyl 2-aminopyridine-4-carboxylate (3.01 g, 19.8 mmol, 2 equiv) and powdered activated 3A sieves (10 g) in ethanol (37 mL) was heated for 4 h at the reflux temperature. The resulting solution was filtered through a pad of Celite with the aid of CH2Cl2. The resulting solution was separated between CH2Cl2 (50 mL) and a saturated aqueous NaHCO3 solution 50 mL). The organic phase was washed with a saturated aqueous NaCl solution, dried (Na2SO4 anh), and concentrated under reduced pressure. The remaining material was purified using MPLC (Biotage Isolera; 100 g SNAP cartridge: 100% hexane for 1.0 min., gradient to 80% hexane/20% EtOAc over 1.0 min., 80% hexane/20% EtOAc for 2.0 min., gradient to 75% hexane/25% EtOAc over 1.0 min., 75% hexane/25% EtOAc for 2.0 min, gradient to 50% hexane/50% EtOAc over 4.0 min., 50% hexane/50% EtOAc for 5.0 min., gradient to 25% hexane/75% EtOAc over 9.5 min.) to give 2-[4-(1-tert-butoxycarbonylamino-cyclobutyl)-phenyl]-3-phenyl-imidazo[1,2-a]pyridine-7-carboxylic acid methyl ester (2.3 g, 47%):
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08975265B2 |
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| 출처 데이터셋 | uspto-grants-2015_03 |
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| ORD ID | ord-da036bc2241b42d9b5662ea8eb3b79c0 |
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| 출처 메모 | uspto-grants-2015_03 |
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