Sodium borohydride → HCID 57936239、化合物
反応式
[CH3:1][C:2]1([CH3:27])[CH2:7][CH:6]([NH:8][C:9]2[N:14]=[C:13]([C:15]3[CH:20]=[CH:19][C:18]([CH2:21][C:22](=[O:24])[CH3:23])=[CH:17][CH:16]=3)[CH:12]=[CH:11][N:10]=2)[CH2:5][C:4]([CH3:26])([CH3:25])[NH:3]1.[BH4-].[Na+]>CO>[CH3:26][C:4]1([CH3:25])[CH2:5][CH:6]([NH:8][C:9]2[N:14]=[C:13]([C:15]3[CH:20]=[CH:19][C:18]([CH2:21][CH:22]([OH:24])[CH3:23])=[CH:17][CH:16]=3)[CH:12]=[CH:11][N:10]=2)[CH2:7][C:2]([CH3:27])([CH3:1])[NH:3]1参加物
4
実験手順
The title compound was prepared by reduction of {4-[2-(2,2,6,6-tetramethyl-piperidin-4-ylamino)-pyrimidin-4-yl]-phenyl}-propan-2-one with sodium borohydride in MeOH. Yield: 32 mg (100%).
出典と根拠
- ORDレコード
- ord-590d389527aa42f5bc9ba155a1f4015d
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07615562B2
反応ノート
読み込み中…