Diisopropylethylamine → 1-(2-Cyclopropyl-acetyl)-piperidine-4-carboxylic acid (4-isopropyl-phenyl)-amide
반응식
[CH:1]1([CH2:4][C:5]([OH:7])=O)[CH2:3][CH2:2]1.C(N(C(C)C)C(C)C)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.[CH:44]([C:47]1[CH:52]=[CH:51][C:50]([NH:53][C:54]([CH:56]2[CH2:61][CH2:60][NH:59][CH2:58][CH2:57]2)=[O:55])=[CH:49][CH:48]=1)([CH3:46])[CH3:45]>C(#N)C>[CH:44]([C:47]1[CH:48]=[CH:49][C:50]([NH:53][C:54]([CH:56]2[CH2:61][CH2:60][N:59]([C:5](=[O:7])[CH2:4][CH:1]3[CH2:2][CH2:3]3)[CH2:58][CH2:57]2)=[O:55])=[CH:51][CH:52]=1)([CH3:46])[CH3:45]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Cyclopropylacetic acid (0.055 g) was dissolved in acetonitrile (6 ml), ethyl-diisopropyl-amine (0.129 g), BOP (0.221 g) was added at RT under an argon atmosphere and the mixture was stirred for 30 minutes at RT. Then piperidine-4-carboxylic acid (4-isopropyl-phenyl)-amide (0.123 g) in acetonitrile (2 ml) was added dropwise at RT and the reaction mixture was stirred for 12 h until completion of the reaction. It was then partitioned between ethyl acetate and aqueous 1M HCl, the layers were separated and the aqueous layer washed with 2M aqueous KHCO3 then dried over Na2SO4. The solvent was evaporated off, the residue purified by flash chromatography (AcOEt/heptane, gradient from 0 to 60%) to give 1-(2-cyclopropyl-acetyl)-piperidine-4-carboxylic acid (4-isopropyl-phenyl)-amide (0.158 g) as an off-white solid. MS (ESI): 329.17 (MH+).
후처리
- stirringthe reaction mixture was stirred for 12 h until completion of the reaction
- customIt was then partitioned between ethyl acetate and aqueous 1M HCl
- customthe layers were separated
- washthe aqueous layer washed with 2M aqueous KHCO3
- dry with materialthen dried over Na2SO4
- customThe solvent was evaporated off
- customthe residue purified by flash chromatography (AcOEt/heptane, gradient from 0 to 60%)
출처 및 근거
- ORD 기록
- ord-97e22edef6894f588d24ba980e2972d5
- 출처 데이터셋
- uspto-grants-2012_09
- 특허 번호
- US08258158B2
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