1-Hydroxybenzotriazole → HCID 178522633, compound
Reaction equation
[OH:1][C:2]1[CH:11]=[C:10]([C:12]([OH:14])=O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.CN(C(ON1[N:31]=[N:30][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29]C1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C1C=CC2N([OH:48])N=NC=2C=1.C[N:50]([C:52]([O:56]N1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C1C=NC2N(O)N=NC=2C=1>>[O:48]1[CH:29]=[CH:28][CH:27]=[C:26]1[C:25]1[O:56][C:52]([NH:50][C:12]([C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([OH:1])[CH:11]=2)=[O:14])=[N:31][N:30]=1Participants
6
Reactant 5
Product 1
Procedure
The title compound was synthesized according to the synthesis method of a compound Ia-46 described later using 2-hydroxy-4-quinolinecarboxylic acid, commercially available amine, HBTU, and HOBt instead of 2-(4-fluorophenyl)-4-quinolinecarboxylic acid, HATU, and HOAt.
Workup
- customaccording to the synthesis method of a compound Ia-46
Sources & evidence
- ORD record
- ord-98256e3ef7264c76951ee9f7f832af0e
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08466290B2
Reaction notes
Loading…