Isocyanatocyclopropane → HCID 66761748, compound
Reaction equation
FC(F)(F)C(O)=O.[CH:8]1([C:13]([N:15]2[CH2:20][CH:19]([C:21]3[CH:26]=[CH:25][C:24]([CH2:27][CH3:28])=[CH:23][CH:22]=3)[CH2:18][CH:17]([NH2:29])[CH2:16]2)=[O:14])[CH2:12][CH2:11][CH2:10][CH2:9]1.[CH:30]1([N:33]=[C:34]=[O:35])[CH2:32][CH2:31]1>>[CH:8]1([C:13]([N:15]2[CH2:20][CH:19]([C:21]3[CH:22]=[CH:23][C:24]([CH2:27][CH3:28])=[CH:25][CH:26]=3)[CH2:18][CH:17]([NH:29][C:34]([NH:33][CH:30]3[CH2:32][CH2:31]3)=[O:35])[CH2:16]2)=[O:14])[CH2:9][CH2:10][CH2:11][CH2:12]1Participants
3
Procedure
108 mg (0.22 mmol) of 1-(cyclopentylcarbonyl)-5-(4-ethylphenyl)piperidine-3-amine trifluoroacetate (Example 7A) and 22 mg (0.26 mmol, 1.2 eq.) of cyclopropyl isocyanate were reacted according to General Method 4. Yield: 64 mg (76% of theory)
Sources & evidence
- ORD record
- ord-9c1e5209869f4ab1ba71687603eedf59
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987248B2
Reaction notes
Loading…