Hydrazine hydrate (1:1) → HCID 60206781, compound
Reaction equation
[N:1]1([CH2:6][CH2:7][NH:8][C:9]([C:11]2[S:15][C:14]([C:16]([O:18]C)=O)=[CH:13][CH:12]=2)=[O:10])[CH2:5][CH2:4][CH2:3][CH2:2]1.O.[NH2:21][NH2:22]>C(O)C>[N:1]1([CH2:6][CH2:7][NH:8][C:9]([C:11]2[S:15][C:14]([C:16]([NH:21][NH2:22])=[O:18])=[CH:13][CH:12]=2)=[O:10])[CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl 5-[2-(pyrrolidin-1-yl)ethylcarbamoyl]-thiophene-2-carboxylate (56 mg, 0.2 mmol) in ethanol (2.0 mL) was refluxed with heating with hydrazine monohydrate (0.10 mL) for 10 hours and allowed to cool to room temperature, and the precipitated solid was collected by filtration, washed with water and dried to give 21 mg of the desired product (yield 38%).
Workup
- filtrationthe precipitated solid was collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-3ced9a2c2f9c4adfacdc7cca263d2135
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08134013B2
Reaction notes
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