Trifluoroacetate → HCID 178526710, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][C@H:9]2[CH2:14][CH2:13][C@H:12]([OH:15])[CH2:11][CH2:10]2)[C:5]([N+:16]([O-:18])=[O:17])=[CH:4][CH:3]=1.FC(F)(F)C([O-])=[O:22]>>[OH:15][C@H:12]1[CH2:13][CH2:14][C@H:9]([NH:8][C:6]2[N:7]=[C:2]([OH:22])[CH:3]=[CH:4][C:5]=2[N+:16]([O-:18])=[O:17])[CH2:10][CH2:11]1Participants
3
Procedure
From trans-4-(6-chloro-3-nitropyridin-2-ylamino)cyclohexanol, trifluoroacetate, prepared in a similar manner as the one described in Example 1.3, Step B, the title compound was obtained. LCMS m/z=254.4 [M+H]+.
Sources & evidence
- ORD record
- ord-bfd49c3feacf4b9388f08dafe87c9e1b
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08507473B2
Reaction notes
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