2-cyclobutylacetic Acid → HCID 59577965, compound
Reaction equation
CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C(O)(=O)C.[F:27][C:28]([F:48])([F:47])[O:29][C:30]1[CH:35]=[CH:34][C:33]([N:36]2[CH2:40][CH2:39][C:38]3([CH2:45][CH2:44][NH:43][CH2:42][CH2:41]3)[C:37]2=[O:46])=[CH:32][CH:31]=1.[CH:49]1([CH2:53][C:54](O)=[O:55])[CH2:52][CH2:51][CH2:50]1>>[CH:49]1([CH2:53][C:54]([N:43]2[CH2:42][CH2:41][C:38]3([C:37](=[O:46])[N:36]([C:33]4[CH:34]=[CH:35][C:30]([O:29][C:28]([F:27])([F:47])[F:48])=[CH:31][CH:32]=4)[CH2:40][CH2:39]3)[CH2:45][CH2:44]2)=[O:55])[CH2:52][CH2:51][CH2:50]1Participants
4
Procedure
The title compound was prepared in analogy to example 13 step A (using TBTU instead of BOP as the coupling reagent) from 2-(4-trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one acetic acid salt (described in example 180 step C) and cyclobutyl-acetic acid. Off-white solid. MS (ESI): 411.3 (MH+).
Sources & evidence
- ORD record
- ord-04122d87d2cd4dc6b9b27433a314d25a
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329904B2
Reaction notes
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