Acetic Acid → 1-[2-carbamoylmethyl-3-mercaptopropanoyl]-L-proline

HRID 1762528Notes

Reaction equation

HRID 1762528 reaction equation
C([S:4][CH2:5][CH:6]([CH2:17][C:18]([O:20]C)=O)[C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8])(=O)C.CO.C(O)(=O)C.[NH3:28]>O>[C:18]([CH2:17][CH:6]([CH2:5][SH:4])[C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8])(=[O:20])[NH2:28]

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 222AmmoniaHCID 887MethanolHCID 541123831-[3-(Acetylthio)-2-(methoxycarbonylmethyl)propanoyl]-L-proline

Product 1

HCID 867357171-[2-carbamoylmethyl-3-mercaptopropanoyl]-L-proline

Reagents, catalysts & solvents 1

HCID 962WaterSolvent2×

Procedure

2.1 g. of the product from Example 81 is dissolved in a mixture of water (40 ml.) and concentrated ammonia (40 ml.). After one hour the reaction mixture is concentrated to 1/3 volume, and applied to a column of Dowex 50 resin in the hydrogen cycle. The product is eluted with water. The aqueous is extracted with ethyl acetate and then concentrated to dryness to yield 1.4 g. of the named product Rf : 0.50 (silica gel-Chloroform:methanol:acetic acid:water).

Workup

  1. concentrationAfter one hour the reaction mixture is concentrated to 1/3 volume
  2. washThe product is eluted with water
  3. extractionThe aqueous is extracted with ethyl acetate
  4. concentrationconcentrated to dryness
  5. customto yield 1.4 g

Sources & evidence

ORD record
ord-3741234f38e845c89becc72bb2c5f896
Source dataset
uspto-grants-1989_05
Patent number
US04833152

Reaction notes

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