Water → HCID 87825019, compound
Reaction equation
[CH2:1]([NH:3][C:4]([C:6]1[C:7]2[CH2:14][CH2:13][CH2:12][C:11](=O)[C:8]=2[S:9][CH:10]=1)=[O:5])[CH3:2].[OH2:16].Cl.[NH2:18]O.C([O-])(=O)C.[Na+]>C(O)C>[CH2:1]([NH:3][C:4]([C:6]1[C:7]2[CH2:14][CH2:13][CH2:12]/[C:11](=[N:18]/[OH:16])/[C:8]=2[S:9][CH:10]=1)=[O:5])[CH3:2]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
A solution of 7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid ethyl amide (the compound of Preparation Example 115) (96 mg) in ethanol (2 mL) and water (1 mL) was added hydroxylamine.hydrochloride (39 mg) and 46 mg of sodium acetate (46 mg). After heating at 50° C. for 4.5 hours, the reaction solution was cooled to room temperature, the solid that precipitated was collected by filtration, and the title compound (36 mg) was obtained as a colorless solid.
Workup
- temperaturethe reaction solution was cooled to room temperature
- customthe solid that precipitated
- filtrationwas collected by filtration
Sources & evidence
- ORD record
- ord-0d8cf0b228c4415aa9650063ef4dfe7a
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07217723B2
Reaction notes
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