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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1874491생성일: 2026년 10월 26일

Tetrahydrofuran → N-[2-chloro-5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)phenyl]-2-methyl-5-(trifluoromethyl)-1,3-oxazole-4-carboxamide

https://huagongshe.com/reaction/1874491

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Thionyl ChlorideHCID 24386—
반응물2-methyl-5-(trifluoromethyl)-1,3-oxazole-4-carboxylic AcidHCID 2775651—
반응물N-[6-(3-amino-4-chlorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamideHCID 57749285—
촉매DimethylformamideHCID 6228—
용매DimethylacetamideHCID 31374—
생성물N-[2-chloro-5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)phenyl]-2-methyl-5-(trifluoromethyl)-1,3-oxazole-4-carboxamideHCID 5774937948.1%

반응 단계

In the same manner as in Example 55 and using 2-methyl-5-(trifluoromethyl)-1,3-oxazole-4-carboxylic acid (110 mg, 0.564 mmol), tetrahydrofuran (5 mL), thionyl chloride (97.2 μL, 1.12 mmol), N,N-dimethylformamide (2 drops), N-[6-(3-amino-4-chlorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (170 mg, 0.495 mmol) and N,N-dimethylacetamide (6 mL) as starting materials, the title compound (124 mg, 48%) was obtained as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304557B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-993ed4cdaa024266a178efdefbb844e3
출처 메모uspto-grants-2012_11