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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388097생성일: 2026년 10월 25일

Triethylamine → 1-Cyclopentylethyl-6-quinolin-5-YL-1,3-dihydro-imidazo[4,5-B]pyrazin-2-one

https://huagongshe.com/reaction/388097

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Cyclopentylmethanamine hydrochlorideHCID 18784136—
반응물1-Cyclopentylmethyl-6-quinolin-5-yl-1,3-dihydro-imidazo[4,5-b]pyrazin-2-oneHCID 66699673—
용매EthanolHCID 702—
생성물1-Cyclopentylethyl-6-quinolin-5-YL-1,3-dihydro-imidazo[4,5-B]pyrazin-2-oneHCID 6743199836%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372976B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-dbd56a38a13d414bb87a91acefd47944
출처 메모uspto-grants-2013_02