Lithium hydroxide, monohydrate → 2-(2-(Benzylcarbamoyl)-1-methylhydrazinyl)acetic acid
Reaction equation
[CH2:1]([N:4]([CH2:16][C:17]([O:19]CC)=[O:18])[NH:5][C:6](=[O:15])[NH:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)C=C.O.[OH-].[Li+]>>[CH2:8]([NH:7][C:6]([NH:5][N:4]([CH2:16][C:17]([OH:19])=[O:18])[CH3:1])=[O:15])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1Participants
3
Procedure
According to the procedure described in the synthesis method of Compound VI-2 with the modification that the reaction was carried out overnight, ethyl 2-(1-allyl-2-(benzylcarbamoyl)hydrazinyl)acetate (Compound V-2) 1.33 g (5.0 mmol) was reacted with lithium hydroxide monohydrate 420 mg (10.0 mmol) to obtain the title compound 1.05 g (88%).
Workup
- customdescribed in the synthesis method of Compound VI-2 with the modification that the reaction
Sources & evidence
- ORD record
- ord-34be39171bbe46d381f393b19a0e2ba8
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09193734B2
Reaction notes
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