Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388089생성일: 2026년 10월 25일
Cyclopentanemethylamine → 1-Cyclopentylethyl-6-(5-isopropyl-2-methoxy-phenyl)-1,3-dihydro-imidazo[4,5-B]pyrazin-2-one
https://huagongshe.com/reaction/388089
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Cyclopentanemethylamine | HCID 80153 | — |
| 반응물 | 1-Cyclopentylmethyl-6-(5-isopropyl-2-methoxy-phenyl)-1,3-dihydro-imidazo[4,5-b]pyrazin-2-one | HCID 24984849 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-Cyclopentylethyl-6-(5-isopropyl-2-methoxy-phenyl)-1,3-dihydro-imidazo[4,5-B]pyrazin-2-one | HCID 67433304 | 75% |
반응 단계
1-Cyclopentylmethyl-6-(5-isopropyl-2-methoxy-phenyl)-1,3-dihydro-imidazo[4,5-b]pyrazin-2-one. N-Bis-Boc-3-bromo-5-(5-isopropyl-2-methoxy-phenyl)-pyrazin-2-ylamine (see Example 5.C) (150 mg, 0.29 mmol), cyclopentylmethylamine (0.287 mL, 2.9 mmol) and ethanol (4 mL) were heated according to General Procedure E. The product was purified using reverse-phase semi-preparatory HPLC (5-70% acetonitrile+0.1% TFA in H2O+0.1% TFA, over 30 min). Product fractions were concentrated and then triturated with 50% methanol in H2O to give a white solid (77 mg, 75% yield). 1H NMR (300 MHz, DMSO-d6) δ 11.98 (s, 1H), 8.36 (s, 1H), 7.60 (d, J=2.5, 1H), 7.26 (dd, J=8.7, 2.6, 1H), 7.08 (d, J=8.5, 1H), 3.82 (s, 3H), 3.78 (d, J=7.4, 2H), 2.45 (d, J=7.1, 1H), 1.58-1.70 (m, 4H), 1.53 (d, J=9.3, 2H), 1.38 (d, J=4.4, 2H), 1.22 (d, J=6.9, 6H); MS (ESI) m/z 367.5 [M+1]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08372976B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-99d4ee393eda4ba48aa5a2ae60cc125e |
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| 출처 메모 | uspto-grants-2013_02 |
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