反応式
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([C:21]3[N:26]=[CH:25][CH:24]=[CH:23][N:22]=3)=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:27]>>[ClH:27].[NH:8]1[CH2:9][CH2:10][CH:11]([NH:14][C:15]2[CH:16]=[CH:17][C:18]([C:21]3[N:22]=[CH:23][CH:24]=[CH:25][N:26]=3)=[CH:19][CH:20]=2)[CH2:12][CH2:13]1参加物
3
実験手順
Stirred 4-(4-Pyrimidin-2-yl-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (110 mg, 0.310 mmol) in 4M HCl (20 ml) at room temperature for 1 hour. Solvent was evaporated yielding desired product piperidin-4-yl-(4-pyrimidin-2-yl-phenyl)-amine, hydrochloride (114 mg).
後処理
- customSolvent was evaporated
出典と根拠
- ORDレコード
- ord-a069523144e74a46bc0076cc7a5df77f
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07807672B2
関連ノート
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