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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410718생성일: 2026년 10월 27일

Riluzole → 1-Methyl-2-(6-trifluoromethoxy-benzothiazol-2-ylamino)-1H-benzoimidazole-5-carboxylic acid methyl amide

https://huagongshe.com/reaction/410718

반응식

참여 물질

역할이름HCID투입량
반응물RiluzoleHCID 5070—
반응물1,1'-ThiocarbonyldiimidazoleHCID 80264—
반응물3-amino-N-methyl-4-(methylamino)benzamideHCID 46344445—
용매1,2-DichloroethaneHCID 11—
생성물1-Methyl-2-(6-trifluoromethoxy-benzothiazol-2-ylamino)-1H-benzoimidazole-5-carboxylic acid methyl amideHCID 771060208.2%

반응 단계

1-Methyl-2-(6-trifluoromethoxy-benzothiazol-2-ylamino)-1H-benzoimidazole-5-carboxylic acid methyl amide (74 mg) was prepared by following General Procedure D starting from 3-amino-N-methyl-4-methylamino-benzamide (460 mg), 2-amino-6-(trifluoromethoxy)benzothiazole (499 mg), 1,1′-thiocarbonyl-diimidazole (454 mg), and EDC (611 mg). LC/MS: m/z 423.0. 1H NMR (DMSO-d6, 400 MHz): δ 12.39 (bs, 1H), 8.42 (s, 1H), 8.09 (s, 1H), 7.93 (s, 1H), 7.75 (d, 2H), 7.50 (d, 1H), 7.36 (d, 1H), 3.68 (bs, 3H), 2.81 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759535B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-ce826afd169b4861b256656dbca0109d
출처 메모uspto-grants-2014_06