Lithium hydroxide, monohydrate → (S)-2-(1-allyl-2-(1-phenylethylcarbamoyl)hydrazinyl)acetic acid

HRID 718887Notes

Reaction equation

HRID 718887 reaction equation
[CH2:1]([N:4]([CH2:17][C:18]([O:20]CC)=[O:19])[NH:5][C:6](=[O:16])[NH:7][C@H:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH3:9])[CH:2]=[CH2:3].O.[OH-].[Li+]>>[CH2:1]([N:4]([CH2:17][C:18]([OH:20])=[O:19])[NH:5][C:6](=[O:16])[NH:7][C@H:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH3:9])[CH:2]=[CH2:3]

Participants

3

Reactant 2

HCID 168937Lithium hydroxide, monohydrateHCID 86652566(S)-ethyl 2-(1-allyl-2-(1-phenylethylcarbamoyl)hydrazinyl)acetate

Product 1

HCID 67075541(S)-2-(1-allyl-2-(1-phenylethylcarbamoyl)hydrazinyl)acetic acidYield 94.4%

Procedure

According to the procedure described in the synthesis method of Compound VI-2 with the modification that the reaction was carried out for 2 hours, (S)-ethyl 2-(1-allyl-2-(1-phenylethylcarbamoyl)hydrazinyl)acetate (Compound V-4) 183 mg (0.6 mmol) was reacted with lithium hydroxide monohydrate 30 mg (0.72 mmol) to obtain the title compound 157 mg (94%).

Workup

  1. customdescribed in the synthesis method of Compound VI-2 with the modification that the reaction

Sources & evidence

ORD record
ord-fce15fd5572f46ef94196446cae77f8f
Source dataset
uspto-grants-2015_11
Patent number
US09193734B2

Reaction notes

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