Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 1-Cyclopentylethyl-6-quinolin-5-YL-1,3-dihydro-imidazo[4,5-B]pyrazin-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Cyclopentylmethanamine hydrochloride | HCID 18784136 | — |
| 반응물 | 1-Cyclopentylmethyl-6-quinolin-5-yl-1,3-dihydro-imidazo[4,5-b]pyrazin-2-one | HCID 66699673 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-Cyclopentylethyl-6-quinolin-5-YL-1,3-dihydro-imidazo[4,5-B]pyrazin-2-one | HCID 67431998 | 36% |
반응 단계
1-Cyclopentylmethyl-6-quinolin-5-yl-1,3-dihydro-imidazo[4,5-b]pyrazin-2-one. A solution of N-bis-boc-3-bromo-5-(quinoline-5-yl)-pyrazin-2-ylamine (150 mg, 0.29 mmol), cyclopentylmethylamine hydrochloride (268 mg, 2 mmol), and triethylamine in ethanol (4 mL) was reacted and purified according to General Procedure E2 to give 25 mg (36% yield) of white solid. 1H NMR (300 MHz, DMSO-d6) δ 8.96 (dd, J=4.1, 1.6, 1H), 8.54-8.61 (m, 2H), 8.12 (d, J=8.2, 1H), 7.77-7.90 (m, 2H), 7.47-7.59 (m, 2H), 3.11-3.19 (m, 2H), 1.98-2.12 (m, 1H), 1.67-1.77 (m, 2H), 1.49-1.65 (m, 4H), 1.15-1.30 (m, 2H); MS (ESI) m/z 346.4 [M+1]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08372976B2 |
| 출처 데이터셋 | uspto-grants-2013_02 |
| ORD ID | ord-dbd56a38a13d414bb87a91acefd47944 |
| 출처 메모 | uspto-grants-2013_02 |