Lithium hydroxide, monohydrate → 2-(1-Methyl-2-((thiophen-2-ylmethyl)carbamoyl)hydrazinyl)acetic acid
Reaction equation
[CH3:1][N:2]([CH2:13][C:14]([O:16]CC)=[O:15])[NH:3][C:4](=[O:12])[NH:5][CH2:6][C:7]1[S:8][CH:9]=[CH:10][CH:11]=1.O.[OH-].[Li+]>>[CH3:1][N:2]([CH2:13][C:14]([OH:16])=[O:15])[NH:3][C:4](=[O:12])[NH:5][CH2:6][C:7]1[S:8][CH:9]=[CH:10][CH:11]=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 for 2 hours, ethyl 2-(1-methyl-2-(thiophen-2-ylmethylcarbamoyl)hydrazinyl)acetate (Compound V-13) 1.38 g (5.1 mmol) was reacted with lithium hydroxide monohydrate 426 mg (10.1 mmol) to obtain the title compound 1.0 g (82%).
Workup
- customdescribed in the synthesis method of Compound VI-2 with the modification that the reaction
Sources & evidence
- ORD record
- ord-07e9952533c94354aba41d12bc9bb63a
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09193734B2
Reaction notes
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