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HRID 410747생성일: 2026년 10월 26일

6-Chloro-2-benzothiazolamine → 2-(6-Chloro-benzothiazol-2-ylamino)-1-methyl-1H-benzoimidazole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/410747

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloro-2-benzothiazolamineHCID 7226—
반응물1,1'-ThiocarbonyldiimidazoleHCID 80264—
반응물Methyl 3-amino-4-(methylamino)benzoateHCID 15586064—
용매1,2-DichloroethaneHCID 11—
생성물2-(6-Chloro-benzothiazol-2-ylamino)-1-methyl-1H-benzoimidazole-5-carboxylic acid methyl esterHCID 5839755475%

반응 단계

2-(6-Chloro-benzothiazol-2-ylamino)-1-methyl-1H-benzoimidazole-5-carboxylic acid methyl ester (842 mg) was prepared by following General Procedure D starting from 3-amino-4-methylamino-benzoic acid methyl ester (650 mg), 2-amino-6-chloro-benzothiazole (556 mg), 1,1′-thiocarbonyldiimidazole (715 mg), and EDC (865 mg). LC/MS: m/z 373.7. 1H NMR (DMSO-d6, 400 MHz): δ 12.39 (bs, 1H), 8.19 (s, 1H), 7.92 (s, 1H), 7.84 (s, 1H), 7.64 (s, 1H), 7.50 (d, 1H), 7.38 (d, 1H), 3.86 (s, 3H), 3.62 (bs, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759535B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-43c9dbbd068d4211a01887a7c84e17f9
출처 메모uspto-grants-2014_06