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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2201172생성일: 2026년 10월 24일

Diethyl Ether → 3-(10-(5-Chlorofuran-2-yl)-1,3-dimethyl-2,4-dioxo-2,3,4,7,8,10-hexahydro-1H-pyrimido[4',5':3,4]pyrrolo[2,1-c][1,4]thiazin-5-yl)benzonitrile

https://huagongshe.com/ko/reaction/2201172

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물5-Chloro-2-furaldehydeHCID 2769630—
반응물Bi(OTf)3HCID 9917655—
반응물3-(6-(2-mercaptoethyl)-1,3-dimethyl-2,4-dioxo-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)benzonitrileHCID 86723417—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물3-(10-(5-Chlorofuran-2-yl)-1,3-dimethyl-2,4-dioxo-2,3,4,7,8,10-hexahydro-1H-pyrimido[4',5':3,4]pyrrolo[2,1-c][1,4]thiazin-5-yl)benzonitrileHCID 77105415—

반응 조건

온도100 °C

반응 단계

A suspension comprising 3-(6-(2-mercaptoethyl)-1,3-dimethyl-2,4-dioxo-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)benzonitrile (Intermediate G) (150 mg, 0.441 mmol), 5-chlorofuran-2-carbaldehyde (57.5 mg, 0.441 mmol) and bismuth triflate (28.9 mg, 0.044 mmol) in toluene (5 ml) was heated to 100° C. for 10 min using microwave radiation. After cooling to RT, the reaction mixture was diluted with EtOAc (25 ml) and washed with water. The layers were separated and the aqueous extracted with EtOAc (3×20 ml). The combined organics were dried over MgSO4, filtered and concentrated to yield a brown oil. Purification was carried out by chromatography on silica eluting with 0-45% EtOAc in iso-hexane. The relevant fraction were combined and concentrated in vacuo to yield a pale yellow oil. Diethyl ether (5 ml) was added to the oil to give a white solid. The solid was isolated by suction filtration to afford the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359381B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-c6e3b904576a4b49a69f45abdbcb2c68
출처 메모uspto-grants-2016_06