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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1879159생성일: 2026년 10월 26일

1-(4-fluorophenyl)-N-methylmethanamine → 2-{6-[(4-Difluoromethoxy-benzyl)-methyl-amino]-pyrazin-2-yl}-4-methyl-thiazole-5-carboxylic acid 4-fluoro-benzylamide

https://huagongshe.com/reaction/1879159

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참여 물질

역할이름HCID투입량
반응물1-(4-fluorophenyl)-N-methylmethanamineHCID 736860—
반응물{[4-(Difluoromethoxy)phenyl]methyl}(methyl)amineHCID 3857668—
반응물2-(6-Iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro benzylamideHCID 86645558—
생성물2-{6-[(4-Difluoromethoxy-benzyl)-methyl-amino]-pyrazin-2-yl}-4-methyl-thiazole-5-carboxylic acid 4-fluoro-benzylamideHCID 2495576580%

반응 단계

Following the procedure described in Example 14, making variations as required to replace 4-fluoro-N-methyl-benzylamine with (4-difluoromethoxy-benzyl)-methyl-amine to react with 2-(6-iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro-benzylamide, the title compound was obtained in 80% yield. 1H NMR (400 MHz, CD2Cl2) δ 8.58 (s, 1H), 8.07 (s, 1H), 7.26-7.37 (m, 4H), 7.00-7.11 (m, 4H), 6.51 (bt, J=76, 64 Hz, 1H, CH—F signal), 6.16 (bs, 1H), 4.82 (s, 2H), 4.54 (d, J=8.0 Hz, 2H), 3.14 (s, 3H), 2.70 (s, 3H); MS (ES+) m/z 514.2 (M+1), Rt=1.63 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08314138B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-3522d5f94d5843a68d701d4745a57c44
출처 메모uspto-grants-2012_11