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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226329생성일: 2026년 10월 25일

Methanesulfonyl chloride → HCID 86603641, 화합물

https://huagongshe.com/reaction/226329

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물(2,3-Dihydro-1-benzofuran-5-yl)methanolHCID 2776158—
반응물ethyl (2E)-3-(6-{(tert-butoxycarbonyl)[(3R)-3-pyrrolidinyl]amino}-3-pyridyl)acrylate dihydrochlorideHCID 86603639—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물HCID 86603641HCID 8660364147.2%

반응 단계

To a mixture of 2,3-dihydro-1-benzofuran-5-ylmethanol (95.1 mg), Et3N (0.120 mL), and THF (3 mL) was added methanesulfonyl chloride (0.053 mL) at 4° C. The reaction mixture was stirred for 3 hours, and added ethyl (2E)-3-(6-{(tert-butoxycarbonyl)[(3R)-3-pyrrolidinyl]amino}-3-pyridyl)acrylate dihydrochloride (250 mg) and Et3N (0.281 mL). After stirring for 2 hours at 60° C., the resulting mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over MgSO4, filtered, and evaporated in vacuo. The residue was purified by column chromatography on silica gel to give ethyl (2E)-3-(6-{(tert-butoxycarbonyl)[(3R)-1-(2,3-dihydro-1-benzofuran-5-ylmethyl)-3-pyrrolidinyl]amino}-3-pyridyl)acrylate (134 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557127B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-921a89893f8a4239a874a3f306929314
출처 메모uspto-grants-2009_07