関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea | HCID 10839478 | — |
| 反応物 | Ethanol hydrochloride | HCID 21887872 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea hydrochloride | HCID 67640260 | — |
反応手順
N-((3R)-1-tert-Butylcarbonylmethyl-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-dimethylaminophenyl)urea (70 g, 136.6 mmol) was taken up in ethanol (1 l) and 2.26M HCl ethanol (63.5 ml, 143.4 mmol) was added dropwise. The mixture was warmed up to 50° C. to afford a clear solution, which was seeded, cooled to 0° C. and stirred at the same temperature overnight. The resultant precipitate was collected by flirtation to provide the title compound as a white crystalline (62.4 g, 82%): top. 181°-184° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05728829 |
|---|
| 出典データセット | uspto-grants-1998_03 |
|---|
| ORD ID | ord-55f511a55d61454a83be8c226edee531 |
|---|
| 出典メモ | uspto-grants-1998_03 |
|---|