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HRID 6237作成日:2026年10月24日

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/ja/reaction/6237

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Sodium AzideHCID 33557—
反応物(1S,9aS) N-[(7-Chloroacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamideHCID 18653087—
溶媒TetrahydrofuranHCID 8028—
溶媒Dichloromethane methanolHCID 21226129—
溶媒Ethylacetate methanolHCID 21584119—
生成物(1S,9aS) N-[(7-Azidoacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo [3,4-a]indol-1-yl)methyl]acetamideHCID 86747041—

反応手順

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##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05247090
出典データセットuspto-grants-1993_09
ORD IDord-344b5d26f989476db51adec38886cea4
出典メモuspto-grants-1993_09