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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1157649생성일: 2026년 10월 27일

2-Thiopheneacetyl chloride → N-{3-[3-(2-chloro-4-pyrimidinyl)-6-methylpyrazolo[1,5-a]pyridin-2-yl]phenyl}-2-(2-thienyl)acetamide

https://huagongshe.com/reaction/1157649

반응식

참여 물질

역할이름HCID투입량
반응물2-Thiopheneacetyl chlorideHCID 162362—
반응물{3-[3-(2-Chloro-4-pyrimidinyl)-6-methylpyrazolo[1,5-a]pyridin-2-yl]phenyl}amineHCID 57737218—
용매TetrahydrofuranHCID 8028—
생성물N-{3-[3-(2-chloro-4-pyrimidinyl)-6-methylpyrazolo[1,5-a]pyridin-2-yl]phenyl}-2-(2-thienyl)acetamideHCID 5773722789.3%

반응 단계

{3-[3-(2-Chloro-4-pyrimidinyl)-6-methylpyrazolo[1,5-a]pyridin-2-yl]phenyl}amine (0.57 g, 1.68 mmol) and 2-thienylacetyl chloride (0.25 mL, 2.00 mmol) were stirred in THF (30 mL) and stirred for 16 h. Additional 2-thienylacetyl chloride was added until reaction was complete by LC/MS. The mixture was concentrated to dryness and partitioned between aqueous NaHCO3 (saturated) and DCM. The organic layers were concentrated and purified by column chromatography to afford N-{3-[3-(2-chloro-4-pyrimidinyl)-6-methylpyrazolo[1,5-a]pyridin-2-yl]phenyl}-2-(2-thienyl)acetamide as a yellow solid (0.69 g, 89%). ES-LC/MS m/z=460 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07807673B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-ecfa4839eb3c4452a2f7958764ab03cc
출처 메모uspto-grants-2010_10