Trifluoroacetic acid → spiro[indene-1,4'-piperidin]-3(2H)-one
Reaction equation
CC(OC([N:8]1[CH2:13][CH2:12][C:11]2([C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[C:15](=[O:16])[CH2:14]2)[CH2:10][CH2:9]1)=O)(C)C.FC(F)(F)C(O)=O>>[NH:8]1[CH2:13][CH2:12][C:11]2([C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[C:15](=[O:16])[CH2:14]2)[CH2:10][CH2:9]1Participants
3
Procedure
N-boc-1-[4-spiro-piperidine]-3-indanone and trifluoroacetic acid were processed according to the method of Example 137D to provide the product. No purification was required. MS (ESI+) m/z 202 (M+H)+.
Workup
- customto provide the product
- customNo purification
Sources & evidence
- ORD record
- ord-3e8e73881c1a404abf5726fe96e938a2
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07704997B1
Reaction notes
Loading…