Hydrochloric Acid → (2S)-2-amino-1-(benzo[d]oxazol-2-yl)butan-1-ol dihydrochloride
反応式
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10]([OH:22])[C@@H:11]([NH:14]C(=O)OC(C)(C)C)[CH2:12][CH3:13].[ClH:23]>O1CCOCC1>[ClH:23].[ClH:23].[NH2:14][C@@H:11]([CH2:12][CH3:13])[CH:10]([C:2]1[O:1][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=1)[OH:22]参加物
4
実験手順
Under an atmosphere of argon, tert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamate (800 mg, 2.61 mmol, Eq: 1.00) and HCl 4M in dioxane (17.3 ml) were combined to give a dark brown solution. The reaction was stirred for 2 h at RT. The crude reaction mixture was concentrated in vacuo, and the residual solvent was removed under vacuum. The title compound was obtained as a dark brown gum (910 mg, quant., MS (m/e)=207.1 [M+H+]).
後処理
- customto give a dark brown solution
- customThe crude reaction mixture
- concentrationwas concentrated in vacuo
- customthe residual solvent was removed under vacuum
出典と根拠
- ORDレコード
- ord-e70eba47d28c4d449340b270008570de
- 出典データセット
- uspto-grants-2014_05
- 特許番号
- US08729061B2
反応ノート
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