関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Butyl chloroformate | HCID 61140 | — |
| 反応物 | HCID 178507852 | HCID 178507852 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | HCID 178452819 | HCID 178452819 | — |
反応手順
20 G. of 2,4-diamino-6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxide are mixed with 250 ml. of methylene chloride and 35 ml. of triethylamine, stirred and cooled to 5° C. The mixture is treated with 45 ml. of chloroformic acid butyl ester and stirred at room temperature for 6 hours. The mixture obtained is washed with water, extracted with methylene chloride and evaporated under reduced pressure. The residue is recystallized from ethanol, there being obtained dibutyl 6-[3,6-dihydro-1(2H)-pyridyl]-2,4-pyrimidine-dicarbamate-3-oxide, having a melting point of 131°-132° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04182867 |
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| 出典データセット | uspto-grants-1980_01 |
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| ORD ID | ord-122818d9cf724bc1a4dbac9aed9b263b |
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| 出典メモ | uspto-grants-1980_01 |
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