Chloroform ethylacetate → HCID 86674621、化合物
反応式
[CH2:1]([NH:8][C:9]1[S:10][C:11]([CH2:14][NH:15][C:16]2[S:17][C:18]([C:21]3[CH:26]=[CH:25][C:24]([CH3:27])=[CH:23][CH:22]=3)=[CH:19][N:20]=2)=[CH:12][N:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)(Cl)[Cl:29].CCOC(C)=O>Cl>[ClH:29].[ClH:29].[CH2:1]([NH:8][C:9]1[S:10][C:11]([CH2:14][NH:15][C:16]2[S:17][C:18]([C:21]3[CH:22]=[CH:23][C:24]([CH3:27])=[CH:25][CH:26]=3)=[CH:19][N:20]=2)=[CH:12][N:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
N-Benzyl-5-((5-p-tolylthiazol-2-ylamino)methyl)thiazol-2-amine (20 mg, 0.05 mmol) was dissolved in methanolic HCl (3 N, 1 mL) and CHCl3/AcOEt was added. The precipitated solid was filtered by decantation and dried in vacuo, yielding N-benzyl-5-((5-p-tolylthiazol-2-ylamino)methyl)thiazol-2-amine dihydrochloride as a white solid (11 mg, 10%). Mp. 105-106° C.
後処理
- filtrationThe precipitated solid was filtered by decantation
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-be9ec0f6f5d14e3e9b3d9ecb3e02da21
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08673940B2
反応ノート
読み込み中…