反応式
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][N:5]=[CH:4][N:3]=1.Cl.[C:10](=N)(OCC)[CH2:11][CH2:12][CH2:13][CH3:14]>CN(C)C=O>[CH2:11]([C:10]1[NH:1][C:2]2[N:3]=[CH:4][N:5]=[CH:6][C:7]=2[N:8]=1)[CH2:12][CH2:13][CH3:14]参加物
4
実験手順
Using the procedure of Example 1, 5 g of 4,5-diaminopyrimidine and 10 g of ethyl pentanimidoate hydrochloride [J.A.C.S., Vol. 64, p 1827 (1942)] using dimethylformamide as solvent were reacted to obtain 2.1 g of the desired product which after crystallization from ethyl acetate melted at 166° C. The product was crystallized from ethyl acetate to obtain 1.8 g of the expected product melting at 168° C. 200 mg of an analytical sample was obtained by an additional crystallization of 300 mg of the product from ethyl acetate melting at 168° C.
後処理
- customwere reacted
出典と根拠
- ORDレコード
- ord-210f4d400a3b450da44784244e0b5696
- 出典データセット
- uspto-grants-1995_02
- 特許番号
- US05389634
関連ノート
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