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HRID 1253348作成日:2026年10月27日

2-Amino-3-Hydroxypyridine → 2-(Chloromethyl)(1,3)oxazolo(4,5-b)pyridine

https://huagongshe.com/reaction/1253348

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-3-HydroxypyridineHCID 28114—
反応物2-Chloro-1,1,1-triethoxyethaneHCID 305922—
溶媒DiglymeHCID 8150—
生成物2-(Chloromethyl)(1,3)oxazolo(4,5-b)pyridineHCID 2764569—

反応手順

The commercially available 2-amino-3-hydroxypyridine (5.0 g) and diglyme (30 ml) were heated at 125° C. to obtain a solution. To this solution was added 2-chloro-1,1,1-triethoxyethane (9.9 g) and the mixture was held at 125° for 1 hour. The solution was cooled to room temperature and then decanted to remove a black byproduct residue. The filtrate was diluted with water (50 ml) and the resulting yellow precipitate was collected (1.5 g). A small sample was crystallized from isopropanol (m.p. 115°-118° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04748280
出典データセットuspto-grants-1988_05
ORD IDord-a776109fe3c24b82833cdd246df189d5
出典メモuspto-grants-1988_05