N-(tert-butoxycarbonyl)glycine → (3S)-1-Cbz-3-{cyclohexyl[(N-BOC)aminoacetyl]amino}pyrrolidine
反応式
[C:1]([N:11]1[CH2:15][CH2:14][C@H:13]([NH:16][CH:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)[CH2:12]1)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].CCN(C(C)C)C(C)C.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[NH:56]([C:61]([O:63][C:64]([CH3:67])([CH3:66])[CH3:65])=[O:62])[CH2:57][C:58](O)=[O:59]>CN(C=O)C>[C:1]([N:11]1[CH2:15][CH2:14][C@H:13]([N:16]([CH:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)[C:58](=[O:59])[CH2:57][NH:56][C:61]([O:63][C:64]([CH3:66])([CH3:65])[CH3:67])=[O:62])[CH2:12]1)([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of (3S)-1-Cbz-3-{cyclohexylamino}pyrrolidine (3.0 g, 10.0 mmol), prepared in Intermediate 2, in DMF (30 mL) were added DIPEA (3.50 mL, 20.0 mmol), HBTU (4.88 g, 13 mmol), BOC-Gly (1.92 g, 11 mmol). After the mixture was stirred at rt for 4 h, the solvent was removed in vacuo, and the residue was diluted with an aqueous NaHCO3. The organic material was extracted with EtOAc, and the organic extracts were washed with 1N HCl, dried over MgSO4, concentrated in vacuo. The residue was purified by column chomatography (EtOAc/Hex=1/3) to give the title compound (4.63 g, 92.0%).
後処理
- customthe solvent was removed in vacuo
- additionthe residue was diluted with an aqueous NaHCO3
- extractionThe organic material was extracted with EtOAc
- washthe organic extracts were washed with 1N HCl
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customThe residue was purified by column chomatography (EtOAc/Hex=1/3)
出典と根拠
- ORDレコード
- ord-996032b83d3546c9a50819abcdee531b
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07989634B2
反応ノート
読み込み中…