1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → tert-butyl(S)-1-(2-(3,5-dichlorophenylamino)acetyl)piperidin-3-ylcarbamate
反応式
[NH:1]1[CH2:6][CH2:5][CH2:4][C@H:3]([NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:2]1.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.[Cl:36][C:37]1[CH:38]=[C:39]([NH:44][CH2:45][C:46](O)=[O:47])[CH:40]=[C:41]([Cl:43])[CH:42]=1.CCN(C(C)C)C(C)C>CN(C=O)C.CCOC(C)=O>[Cl:36][C:37]1[CH:38]=[C:39]([NH:44][CH2:45][C:46]([N:1]2[CH2:6][CH2:5][CH2:4][C@H:3]([NH:7][C:8](=[O:14])[O:9][C:10]([CH3:11])([CH3:13])[CH3:12])[CH2:2]2)=[O:47])[CH:40]=[C:41]([Cl:43])[CH:42]=1参加物
8
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of tert-butyl(S)-piperidin-3-ylcarbamate (500 mg, 2.5 mmol), in DMF (5 mL) was added EDCI (573 mg, 3.0 mmol), HOBt (405 mg, 3.0 mmol), 2-(3,5-dichlorophenylamino)acetic acid (550 mg, 2.5 mmol) and DIEA (0.5 mL, 3.0 mmol) at 0° C. The reaction mixture was stirred at rt overnight, the reaction mixture was diluted with EtOAc and washed with water. The water layer was extracted with the EtOAc and the combined organic layer was dried over Na2SO4 and evaporated in vacuo to give the crude compound that was purified by column chromatography (silica gel, gradient MeOH in CH2Cl2) to afford (900 mg, 98%) of the titled intermediate. LCMS: m/z: [M+1]=402.
後処理
- washwashed with water
- extractionThe water layer was extracted with the EtOAc
- dry with materialthe combined organic layer was dried over Na2SO4
- customevaporated in vacuo
- customto give the crude compound that
- customwas purified by column chromatography (silica gel, gradient MeOH in CH2Cl2)
出典と根拠
- ORDレコード
- ord-86850e8ba64545f0ad05abdb7aac3483
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09273028B2
反応ノート
読み込み中…