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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 749198생성일: 2026년 10월 26일

Dichloromethane → 3-{[7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl]amino}-N-(3-fluorophenyl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/749198

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물1,4-DioxaneHCID 31275—
반응물4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazolineHCID 57447227—
반응물3-amino-N-(3-fluorophenyl)-1H-pyrazole-5-carboxamideHCID 64523814—
용매Hydrochloric AcidHCID 313—
용매DimethylacetamideHCID 31374—
생성물3-{[7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl]amino}-N-(3-fluorophenyl)-1H-pyrazole-5-carboxamideHCID 6898746188%

반응 단계

3-Amino-N-(3-fluorophenyl)-1H-pyrazole-5-carboxamide (153 mg, 0.69 mmol) in dimethylacetamide (1.8 ml) and HCl in dioxane (4 M solution in dioxane, 174 μl, 0.69 mmol) was reacted with 4-chloro-7-(3-chloropropoxy)-6-methoxyquinazoline (200 mg, 0.69 mmol) at 90° C. for 1.5 hour. Dichloromethane (35 ml) was added to the cooled reaction mixture, and the solid recovered by filtration, washed with dichloromethane and dried to yield 3-{[7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl]amino}-N-(3-fluorophenyl)-1H-pyrazole-5-carboxamide (286 mg, 81% yield):

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402585B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-4dc25890c54c435fb884c5cabd4bf5ab
출처 메모uspto-grants-2008_07