1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → 1-Benzyl-4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine

HRID 380532ノート

反応式

HRID 380532 の反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH:15]([OH:23])[CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:24]1([C@H:30]([CH3:34])[C:31](O)=[O:32])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.Cl.CN(C)CCCN=C=NCC>C(Cl)Cl.CN(C)C1C=CN=CC=1>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH:15]([O:23][C:31](=[O:32])[C@H:30]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH3:34])[CH2:16][C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH2:10][CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

6

反応物 3

HCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27246222-Phenylpropionic acid, (+)-HCID 183647871-Benzyl-4-(3-phenyl-2-hydroxypropyl)piperidine

生成物 1

HCID 599707671-Benzyl-4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of 1 g (3.23 mmol) of 1-benzyl-4-(3-phenyl-2-hydroxypropyl)piperidine (Example 228, Step 2) and 0.775 g (5.16 mmol) of (S)-2-phenylpropionic acid in 10 mL of CH2Cl2 at 0° C. was added 1.32 g (6.9 mmol) of 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride and 0.1 g of 4-(dimethylamino)pyridine. The reaction was stirred for 5 h and let warm to rt. To the reaction mixture was added 80 mL of CH2Cl2 and the mixture was washed three times with 10% NaOH solution. The organic layer was washed with sat'd NaCl solution, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes:ethyl acetate, 4:1) to give isomer 1a of the the title compound. Mass Spectrum (ESI) m/e=442 (M+1). [α]D=−3.7 (c=2.44, CHCl3).

後処理

  1. washthe mixture was washed three times with 10% NaOH solution
  2. washThe organic layer was washed with sat'd NaCl solution
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated
  6. customThe residue was purified by chromatography (silica, hexanes:ethyl acetate, 4:1)

出典と根拠

ORDレコード
ord-c3d1f61766b34d54bddfaa9103bbab75
出典データセット
uspto-grants-2001_10
特許番号
US06303593B1

反応ノート

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