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HRID 6237생성일: 2026년 10월 23일

Acetone → (1S,9aS) N-[(7-Azidoacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo [3,4-a]indol-1-yl)methyl]acetamide

https://huagongshe.com/ko/reaction/6237

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Sodium AzideHCID 33557—
반응물(1S,9aS) N-[(7-Chloroacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamideHCID 18653087—
용매TetrahydrofuranHCID 8028—
용매Dichloromethane methanolHCID 21226129—
용매Ethylacetate methanolHCID 21584119—
생성물(1S,9aS) N-[(7-Azidoacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo [3,4-a]indol-1-yl)methyl]acetamideHCID 86747041—

반응 단계

A mixture of (1S,9aS) N-[(7-chloroacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamide (EXAMPLE 48, 43 mg) and sodium azide (82 mg) are stirred in aqueous tetrahydrofuran (66%) for 3 days. Acetone (1 ml) is added and the mixture was heated in an oil bath (38°-50°) for 8 hours then concentrated to an aqueous layer and extracted with ethylacetate (6×2 ml). The combined organic layers are dried over magnesium sulfate and concentrated to provide the product as as an oil. The oil is taken up in methylene chloride/methanol and then placed on a 100 μsilica preprative plate and developed in methanol/ethylacetate (10/90, 2×) to give the title compound. ##STR2##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05247090
출처 데이터셋uspto-grants-1993_09
ORD IDord-344b5d26f989476db51adec38886cea4
출처 메모uspto-grants-1993_09