Hydrochloric Acid → 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine

HRID 276112

反応式

HRID 276112 の反応式
C[O:2][C:3](=[O:30])[C@H:4]([CH2:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[NH:5][C:6](=[O:21])[CH:7]([S:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1)[CH2:8][CH2:9][CH3:10].CO.[OH-].[Li+].Cl>CCCCCC.C(OCC)(=O)C.O1CCCC1>[CH3:20][O:19][C:16]1[CH:15]=[CH:14][C:13]([CH2:12][S:11][CH:7]([CH2:8][CH2:9][CH3:10])[C:6]([NH:5][C@H:4]([C:3]([OH:30])=[O:2])[CH2:22][CH2:23][C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)=[O:21])=[CH:18][CH:17]=1

参加物

7

実験手順

Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester (3.50 g, 8.15 mmol) and methanol (30 mL)and tetrahydrofuran (30 (mL). Cool in an ice bath. Add an aqueous 2M lithium hydroxide solution (8.2 mL, 16.4 mmol). After 18 hours, adjust the pH to about 6 using an aqueous 10% hydrochloric acid solution and evaporate in vacuo to give a residue. Partition the residue between dichloromethane and water, adjust the pH of the aqueous layer to about 1 using an aqueous 10% hydrochloric acid solution. Separate the layers, extract the aqueous layer repeatedly with ethyl acetate. Combine the organic layers, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 95% 1/1 hexane/ethyl acetate/5% acetic acid to give the title compound.

後処理

  1. temperatureCool in an ice bath
  2. customevaporate in vacuo
  3. customto give a residue
  4. customPartition the residue between dichloromethane and water
  5. customSeparate the layers
  6. extractionextract the aqueous layer repeatedly with ethyl acetate
  7. dry with materialdry over Na2SO4
  8. filtrationfilter
  9. customevaporate in vacuo
  10. customto give a residue

出典と根拠

ORDレコード
ord-222d2ac6f50248dabfb0e58127fe60d6
出典データセット
uspto-grants-2002_03
特許番号
US06352976B1

関連ノート

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