Cyclopentanecarboxylic acid → N-(1-propyl-1H-tetrazol-5-yl)cyclopentane-carboxamide
Reaction equation
[CH:1]1([C:6]([OH:8])=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:9]([N:12]1[C:16]([NH2:17])=[N:15][N:14]=[N:13]1)[CH2:10][CH3:11]>>[CH2:9]([N:12]1[C:16]([NH:17][C:6]([CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5]2)=[O:8])=[N:15][N:14]=[N:13]1)[CH2:10][CH3:11]Participants
3
Procedure
Employing 0.30 g (2.6 mmol) of cyclopentane carboxylic acid and 0.33 mg (2.6 mmol) of 1-propyl-1H-tetrazol-5-amine in the procedure described above and elution with CH2Cl2/MeOH/Et3N (9.3:0.5:0.2) gave the product in 45% yield.
Workup
- washelution with CH2Cl2/MeOH/Et3N (9.3:0.5:0.2)
- customgave the product in 45% yield
Sources & evidence
- ORD record
- ord-016b7303ec40435695338055668303a2
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975288B2
Reaction notes
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