Hydrazine hydrate (1:1) → HCID 13116743, compound
Reaction equation
[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]2[S:15][C:14]([C:16](=O)[CH2:17][CH2:18][C:19]([OH:21])=O)=[CH:13][CH:12]=2)[CH:5]=[CH:4][N:3]=[CH:2]1.O.[NH2:24][NH2:25]>O>[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]2[S:15][C:14]([C:16]3[CH2:17][CH2:18][C:19](=[O:21])[NH:24][N:25]=3)=[CH:13][CH:12]=2)[CH:5]=[CH:4][N:3]=[CH:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
3.2 g of 4-{5-[5-(1-imidazolyl)-pentyl]-thien-2-yl}-4-oxo-butyric acid are suspended in 10 ml of water, 0.52 g of hydrazine hydrate are added and the mixture is stirred at 90° C. for 2 hours. After the mixture has been cooled, the precipitate formed is filtered off with suction, washed with water and dried.
Workup
- temperatureAfter the mixture has been cooled
- customthe precipitate formed
- filtrationis filtered off with suction
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-94a2f62f977e409e98731f56ddec9039
- Source dataset
- uspto-grants-1985_03
- Patent number
- US04504479
Reaction notes
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