Hydrochloric Acid → HCID 11716529, compound

HRID 1436943Notes

Reaction equation

HRID 1436943 reaction equation
[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:19])[CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4].[ClH:23]>>[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:18])[CH3:19])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4].[ClH:23].[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:18])[CH3:19])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 11716529HCID 11716529, compound

Product 2

HCID 11716529HCID 11716529, compoundHCID 57462857HCID 57462857, compound

Procedure

The hydrochloride salt of (S)-2-amino-3-(2,6-diisopropylphenoxycarbonyloxy)-propanoic acid was prepared by dissolving compound (3) in excess aqueous 1 N hydrochloric acid solution, freezing and then lyophilizing the solution to afford the desired product as an amorphous white solid.

Sources & evidence

ORD record
ord-03dca5fac796452e892a3d13b075cca7
Source dataset
uspto-grants-2009_11
Patent number
US07619110B2

Reaction notes

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