Hydrochloric Acid → 1-Acetyl-6'-benzyl-1',2'-dihydrospiro[azetidine-3,3'-indole]hydrochloride
反応式
C(OC([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([CH2:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:15]=2)[C:10]2([CH2:26][N:25]([C:27](=[O:29])[CH3:28])[CH2:24]2)[CH2:9]1)=O)(C)(C)C.[ClH:30]>CCOC(C)=O>[ClH:30].[C:27]([N:25]1[CH2:24][C:10]2([C:11]3[C:16](=[CH:15][C:14]([CH2:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)=[CH:13][CH:12]=3)[NH:8][CH2:9]2)[CH2:26]1)(=[O:29])[CH3:28]参加物
4
実験手順
1-Acetyl-6′-benzyl-1′,2′-dihydrospiro[azetidine-3,3′-indole]-1′-yl-carboxylic acid tert-butyl ester was taken up in saturated HCl in EtOAc (5 mL). The reaction was stirred for 1 h at ambient temperature and then concentrated in vacuo. The residue was taken up in MeOH and concentrated in vacuo again to yield the title compound. MS: [M+H]+=293.
後処理
- concentrationconcentrated in vacuo
- concentrationconcentrated in vacuo again
出典と根拠
- ORDレコード
- ord-16860118b03344e4bd66be3ecca88145
- 出典データセット
- uspto-grants-2015_04
- 特許番号
- US09018214B2
反応ノート
読み込み中…