Ethanol → HCID 22175261, compound

HRID 1797688Notes

Reaction equation

HRID 1797688 reaction equation
[CH:1]1[C:13]2[CH:12]([CH2:14][O:15][C:16](=[O:42])[NH:17][CH2:18][C:19]3[N:20]([CH2:38][CH:39]([CH3:41])[CH3:40])[C:21](=[O:37])[C:22]4[C:27]([C:28]=3[O:29][CH2:30][CH2:31][CH2:32][CH3:33])=[CH:26][C:25]([C:34]([NH2:36])=[S:35])=[CH:24][CH:23]=4)[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.Cl[CH2:44][C:45]([O:47][CH2:48][CH3:49])=[O:46].O.[CH2:51](O)[CH3:52]>>[CH2:30]([O:29][C:28]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([C:34]3[S:35][C:44]([C:45]([O:47][CH2:48][CH3:49])=[O:46])=[C:51]([CH3:52])[N:36]=3)[CH:26]=2)[C:21](=[O:37])[N:20]([CH2:38][CH:39]([CH3:41])[CH3:40])[C:19]=1[CH2:18][NH:17][C:16]([O:15][CH2:14][CH:12]1[C:11]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=2[C:5]2[C:13]1=[CH:1][CH:2]=[CH:3][CH:4]=2)=[O:42])[CH2:31][CH2:32][CH3:33]

Participants

5

Reactant 4

HCID 702EthanolHCID 962WaterHCID 7751Ethyl chloroacetateHCID 22176325HCID 22176325, compound

Product 1

HCID 22175261HCID 22175261, compoundYield 65.3%

Procedure

A solution of 9H-fluoren-9-ylmethyl[6-(aminocarbothioyl)-4-butoxy-2-isobutyl-1-oxo-1,2-dihydro-3-isoquinolinyl]methylcarbamate (2.33 g, 4 mmol) and ethyl 2-chloroacetate (1.32 g, 8 mmol) in ethanol (20 ml) was refluxed under heating for 10 h. The resulting reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give ethyl 2-[4-butoxy-3-({[(9H-fluoren-9-ylmethoxy)carbonyl]amino}methyl)-2-isobutyl-1-oxo-1,2-dihydro-6-isoquinolinyl]-4methyl-1,3-thiazole-5-carboxylate (1.81 g, 65.3%) as crystals.

Workup

  1. temperatureunder heating for 10 h
  2. customThe resulting reaction mixture
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-5f075d5c1d8d4476972c55e4eeee85ef
Source dataset
uspto-grants-2006_04
Patent number
US07034039B2

Reaction notes

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