関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-[[(Diisopropylamino)methylene]amino]-3-pyridinol | HCID 15380931 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-[[(Diisopropylamino)methylene]amino]-3-pyridinol N,N-dimethyl carbamate | HCID 67749083 | — |
反応手順
To a stirred mixture of 4-[[(diisopropylamino)methylene]amino]-3-pyridinol (1.06 g) and triethylamine (1.0 ml) in 25 ml dry Et2O was added dimethyl carbamyl chloride (0.53 ml). The mixture was stirred at room temperature for 2 hours, after which no starting material remained as seen by TLC (silica, 10:90 CH3OH:CH2Cl2). The mixture was diluted with 25 ml Et2O, filtered, washed with Et2O, and the filtrate concentrated in vacuo and chromatography on silica using EtOAc eluent. The fractions containing desired product were combined and concentrated to provide 500 mg of pure product. Another run was carried out in the same manner as above using 740 mg of starting material. The products from both runs were combined. Recrystallization attempts failed, and the product was dried in vacuo to provide 790 mg of a white solid, m.p. 76°-79° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05821239 |
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| 出典データセット | uspto-grants-1998_10 |
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| ORD ID | ord-8e4e4814a5c44f3bad47ba701a7928ff |
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| 出典メモ | uspto-grants-1998_10 |
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