HCID 86693023, compound → HCID 67516507, compound
Reaction equation
CC(C)(C)C([NH:5][C:6]1[N:11]=[CH:10][C:9]2[CH:12]([C:15]([O-:17])=[O:16])[CH2:13][CH2:14][C:8]=2[CH:7]=1)=O>Cl>[NH2:5][C:6]1[N:11]=[CH:10][C:9]2[CH:12]([C:15]([OH:17])=[O:16])[CH2:13][CH2:14][C:8]=2[CH:7]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3-[(2,2-dimethylpropanoyl)amino]-6,7-dihydro-5H-cyclopenta[c]pyridine-7-carboxylate (0.624 mg, 1.96 mmol) in 6N hydrochloric acid (25 mL) was heated to reflux for 24 h. The solution was cooled and concentrated to provide 3-amino-6,7-dihydro-5H-cyclopenta[c]pyridine-7-carboxylic acid which was used without further purification in the next step. LC/MS (M+1)+=179.0;
Workup
- temperatureto reflux for 24 h
- temperatureThe solution was cooled
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-17eba7f97a9c4a6fb9cee33013b3c4a3
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09056859B2
Reaction notes
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