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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1262365생성일: 2026년 10월 26일

5-Amino-2-(trifluoromethyl)benzimidazole → [7-(4-Methanesulfonyl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-(2-trifluoromethyl-3H-benzimidazol-5-yl)-amine

https://huagongshe.com/reaction/1262365

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-2-(trifluoromethyl)benzimidazoleHCID 19345—
반응물HCID 66711046HCID 66711046—
생성물[7-(4-Methanesulfonyl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-(2-trifluoromethyl-3H-benzimidazol-5-yl)-amineHCID 66712247—

반응 단계

Following the synthetic and purification procedures described in Example 1293d, 2-methanesulfinyl-7-(4-methanesulfonyl-phenyl)-pyrrolo[2,1-f][1,2,4]triazine (75 mg, 0.22 mmol) was coupled with 2-trifluoromethyl-3H-benzimidazol-5-ylamine (78 mg, 0.38 mmol) at 105° C. for 86 h to afford the title compound. Yield of TFA salt: 34 mg (26%) of brown powder; LC/MS: 473 (M+H); HPLC: 95% pure, RT=2.99 min; 1H NMR: (DMSO, δ) 9.73 (s, 1H), 9.09 (s, 1H), 8.51 (d, J=8.4, 2H), 8.40 (s, 1H), 8.13 (br s, 1H), 8.04 (d, J=8.4, 2H), 7.71 (m, 2H), 7.38 (d, J=4.9, 1H), 7.03 (d, J=4.9, 1H), 3.28 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08471005B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-060a73472b9a4b1b83a832165498cc86
출처 메모uspto-grants-2013_06