Ammonia → HCID 178513947, compound
Reaction equation
[C:1]1([NH:7][C@@H:8]2[CH2:13][CH2:12][C@H:11]([C:14]([O:16]C)=O)[CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH3:18]>>[C:1]1([NH:7][C@@H:8]2[CH2:13][CH2:12][C@H:11]([C:14]([NH2:18])=[O:16])[CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
cis-Methyl 4-(phenylamino)cyclohexanecarboxylate (0.50 g, 2.14 mmol) was dissolved in methanolic ammonia (15 ml) in a pressure bomb and heated at 100° C. for three days. The reaction mixture was cooled to room temperature and concentrated under reduced pressure to afford the crude compound which was washed with n-pentane and dried in vacuo to afford 300 mg (63%) of cis-4-(phenylamino)cyclohexanecarboxamide as white solid.
Workup
- temperatureThe reaction mixture was cooled to room temperature
- concentrationconcentrated under reduced pressure
- customto afford the crude compound which
- washwas washed with n-pentane
- customdried in vacuo
Sources & evidence
- ORD record
- ord-3b98ed4fe737487cb0b010ad3d694a9e
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08518948B2
Reaction notes
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