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2-Amino-3-Hydroxypyridine → 2-(Chloromethyl)(1,3)oxazolo(4,5-b)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Amino-3-Hydroxypyridine | HCID 28114 | — |
| 反応物 | 2-Chloro-1,1,1-triethoxyethane | HCID 305922 | — |
| 溶媒 | Diglyme | HCID 8150 | — |
| 生成物 | 2-(Chloromethyl)(1,3)oxazolo(4,5-b)pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04723010 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-3b3a232422e4466d95c7b4b7201b4772 |
| 出典メモ | uspto-grants-1988_02 |