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2,6-Dimethyl-4-aminopyrimidine → HCID 13176760、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,6-Dimethyl-4-aminopyrimidine | HCID 68039 | — |
| 反応物 | Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester | HCID 156281 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | HCID 13176760 | HCID 13176760 | — |
反応手順
To a suspension of 1.2 g of 4-amino-2,6-dimethylpyrimidine in 30 ml of dry acetonitrile with stirring was added 2.4 of 2-methoxycarbonylbenzenesulfonylisocyanate. The mixture was stirred for two hours at ambient temperature, allowed to stand for sixteen hours and the desired product, which had precipitated, was removed by filtration and washed with butyl chloride to yield 2.4 g, m.p. 125°-127°. The product showed absorption peaks by Nuclear Magnetic Resource at 4.0, 2.62 and 2.9 ppm; consistent for the product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04545808 |
| 出典データセット | uspto-grants-1985_10 |
| ORD ID | ord-2e6cfcd7cf0d4a63a94f4be71ba7e0ff |
| 出典メモ | uspto-grants-1985_10 |