関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4,6-Dichloro-5-nitropyrimidine | HCID 20312 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2-Chloroethylamine hydrochloride | HCID 9793737 | — |
| 反応物 | 5-Nitro-4,6-bis(beta-chloroethyl)pyrimidine | HCID 21320077 | — |
| 反応物 | 4-(beta-Chloroethylamino)-5-nitro-6-chloropyrimidine | HCID 21320112 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | HCID 178526808 | HCID 178526808 | — |
反応手順
A solution of 20 g. of 4,6-dichloro-5-nitropyrimidine was prepared in ether. An aqueous solution containing 14 g. of β-chloroethylamine hydrochloride and 24 g. of sodium bicarbonate were added thereto and the subsequent mixture agitated for about 30 minutes. The ether layer was separated, and the separated layer washed with water and dried. Removal of the ether in vacuo yielded an oil containing chiefly 4-(β-chloroethylamino)-5-nitro-6-chloropyrimidine plus a small quantity of 5-nitro-4,6-bis(β-chloroethyl)pyrimidine (the disubstituted product) and a very small quantity of starting material. The oily residue was allowed to stand in chloroform for about one day. A solid comprising 7-(β-chloroethylamino)-8-nitro-2,3-dihydroimidazo[1,2-c]pyrimidine hydrochloride precipitated and the precipitate was separated by filtration, 7-(β-chloroethyl)amino-8-nitro-2,3-dihydroimidazo[1,2-c]pyrimidine hydrochloride thus prepared decomposed at 135° C. after recrystallization from chloroform; yield=5.378 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04153695 |
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| 出典データセット | uspto-grants-1979_05 |
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| ORD ID | ord-a6cb9de849fe45bd9d458bc5c047d3d7 |
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| 出典メモ | uspto-grants-1979_05 |
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