Sodium Iodide → N-(2-Acetylthio-3-methoxybenzoyl)-N-cyclopentylglycine

HRID 67901ノート

反応式

HRID 67901 の反応式
C1(N=C=NC2CCCCC2)CCCCC1.[C:16]([S:19][C:20]1[C:28]([O:29][CH3:30])=[CH:27][CH:26]=[CH:25][C:21]=1[C:22]([OH:24])=O)(=[O:18])[CH3:17].C([O:35][C:36](=[O:44])[CH2:37][NH:38][CH:39]1[CH2:43][CH2:42][CH2:41][CH2:40]1)(C)(C)C.[I-].[Na+].Cl[Si](C)(C)C>C(Cl)Cl.C(#N)C>[C:16]([S:19][C:20]1[C:28]([O:29][CH3:30])=[CH:27][CH:26]=[CH:25][C:21]=1[C:22]([N:38]([CH:39]1[CH2:43][CH2:42][CH2:41][CH2:40]1)[CH2:37][C:36]([OH:44])=[O:35])=[O:24])(=[O:18])[CH3:17]

参加物

8

反応物 5

HCID 5238Sodium IodideHCID 6397ChlorotrimethylsilaneHCID 10868DicyclohexylcarbodiimideHCID 13298943Tert-butyl 2-(cyclopentylamino)acetateHCID 204652112-Acetylthio-3-methoxybenzoic acid

生成物 1

HCID 20465214N-(2-Acetylthio-3-methoxybenzoyl)-N-cyclopentylglycine

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

N,N'-Dicyclohexylcarbodiimide (10.3 g, 50 mmol) in methylene chloride (80 ml) was added to 2-acetylthio-3-methoxybenzoic acid (11.3 g, 50 mmol) and N-cyclopentylglycine t-butyl ester (10.0 g, 50 mmol) in methylene chloride (300 ml) at 0°-5° C. Overnight stirring was followed by filtration and washing of the filtrate with dilute hydrochloric acid, sodium bicarbonate solution and brine. Dryng and concentration gave a gum which was dissolved in acetonitrile (65 ml), combined with sodium iodide (11.2 g, 75 mmol) and heated to 40°-50° C. Chlorotrimethylsilane (8.1 g, 75 mmol) was introduced and the mixture was heated for 30 minutes, then quenched with water. The organic phase was washed with water, aqueous sodium thiosulfate and brine then concentrated. Aqueous sodium bicarbonate was added to the residue and the resulting solution was washed with methylene chloride and ether, then acidified and extracted with ethyl acetate. The organic portion was dried and concentrated and the residue passed through a silica gel column to provide the amorphous product.

後処理

  1. filtrationwas followed by filtration
  2. washwashing of the filtrate with dilute hydrochloric acid, sodium bicarbonate solution and brine
  3. concentrationDryng and concentration
  4. customgave a gum which
  5. temperatureheated to 40°-50° C
  6. temperaturethe mixture was heated for 30 minutes
  7. customquenched with water
  8. washThe organic phase was washed with water, aqueous sodium thiosulfate and brine
  9. concentrationthen concentrated
  10. additionAqueous sodium bicarbonate was added to the residue
  11. washthe resulting solution was washed with methylene chloride and ether
  12. extractionextracted with ethyl acetate
  13. customThe organic portion was dried
  14. concentrationconcentrated
  15. customto provide the amorphous product

出典と根拠

ORDレコード
ord-e37bdb1735b74f2ea41b3cf6844533db
出典データセット
uspto-grants-1982_08
特許番号
US04347246

反応ノート

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