3-Carboxybenzaldehyde → [(1S)-2-(3,5-Dichloro-1-oxido-pyridin-1-ium-4-yl)-1-(3,4-dimethoxyphenyl)ethyl]3-formylbenzoate

HRID 1529522노트

반응식

HRID 1529522 반응식
[Cl:1][C:2]1[CH:3]=[N+:4]([O-:22])[CH:5]=[C:6]([Cl:21])[C:7]=1[CH2:8][C@@H:9]([C:11]1[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[C:13]([O:19][CH3:20])[CH:12]=1)[OH:10].[CH:23]([C:25]1[CH:26]=[C:27]([CH:31]=[CH:32][CH:33]=1)[C:28](O)=[O:29])=[O:24].Cl.CN(C)CCCN=C=NCC>CN(C)C1C=CN=CC=1.C(Cl)Cl>[Cl:21][C:6]1[CH:5]=[N+:4]([O-:22])[CH:3]=[C:2]([Cl:1])[C:7]=1[CH2:8][C@@H:9]([C:11]1[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[C:13]([O:19][CH3:20])[CH:12]=1)[O:10][C:28](=[O:29])[C:27]1[CH:31]=[CH:32][CH:33]=[C:25]([CH:23]=[O:24])[CH:26]=1

참가 물질

6

실험 절차

A solution of (5)-3,5-dichloro-4-(2-(3,4-dimethoxyphenyl)-2-hydroxyethyl)-pyridine 1-oxide (0.688 g, 2 mmol), 3-formylbenzoic acid (0.300 g, 2 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.767 g, 4 mmol) and 4-(dimethylamino)pyridine (0.122 g, 1 mmol) in anhydrous DCM (30 mL) was stirred at RT for 21 hours. The reaction mixture was partitioned between saturated NaHCO3 (20 mL) and DCM (10 mL) and filtered through a phase separator cartridge. The cartridge was washed thoroughly with DCM and the solvent was removed in vacuo. The crude material was purified by silica gel column chromatography eluting with 1:1 DCM:EtOAc to afford the title compound as an off-white solid (0.863 g, 91%).

후처리

  1. customThe reaction mixture was partitioned between saturated NaHCO3 (20 mL) and DCM (10 mL)
  2. filtrationfiltered through a phase separator cartridge
  3. washThe cartridge was washed thoroughly with DCM
  4. customthe solvent was removed in vacuo
  5. customThe crude material was purified by silica gel column chromatography
  6. washeluting with 1:1 DCM

출처 및 근거

ORD 기록
ord-f73fe0cd48ae484ea41d9123ab34960e
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09090606B2

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