Acetic Acid → HCID 178517719、化合物
反応式
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([N:7]2[CH2:12][CH2:11][O:10][CH2:9][CH2:8]2)[N:3]=1.Cl.[CH2:14](N1CCC(C(OCC)=O)C(=O)C1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[C:33]([OH:36])(=O)[CH3:34].[N:37]1C=[CH:41][CH:40]=[CH:39][CH:38]=1>O.CC(C)=O>[CH2:14]([CH:39]1[C:40]2[CH2:41][N:6]3[NH:5][C:4]([N:7]4[CH2:8][CH2:9][O:10][CH2:11][CH2:12]4)=[N:3][C:2]3=[N:1][C:34]=2[C:33](=[O:36])[NH:37][CH2:38]1)[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1参加物
実験手順
A mixture of 50.8 g (0.3 mole) of 5-amino-3-morpholino-1H-1,2,4-triazole, 89.3 g (0.3 mole) of 1-benzyl-4-carbethoxy-3-oxo-piperidine-hydrochloride and 220 ml of acetic acid is refluxed for 7 hours under stirring. The reaction mixture is allowed to stand overnight, the precipitate is filtered and washed with acetone. The product thus obtained is dissolved in a mixture of 400 ml of water and 100 ml of pyridine under heating to boiling for 15 minutes. The solution is allowed to stand for a day, the precipitated crystals are filtered and washed with acetone. The product thus obtained (83.9 g) is dissolved in 260 ml of hot pyridine, to the solution 1000 ml of acetone are added. The precipitated crystals are filtered and washed with acetone. Thus 78.9 g of the desired compound are obtained, yield 72%, m.p.: 315°-317° C.
後処理
- temperatureis refluxed for 7 hours
- filtrationthe precipitate is filtered
- washwashed with acetone
- customThe product thus obtained
- temperatureunder heating
- waitto boiling for 15 minutes
- waitto stand for a day
- filtrationthe precipitated crystals are filtered
- washwashed with acetone
- customThe product thus obtained (83.9 g)
- additionare added
- filtrationThe precipitated crystals are filtered
- washwashed with acetone
出典と根拠
- ORDレコード
- ord-d442ff68ea8a4507bac7f54d43aa8b86
- 出典データセット
- uspto-grants-1989_05
- 特許番号
- US04831029
反応ノート
読み込み中…