2,4-Difluorobenzoic acid → HCID 22507717, compound
Reaction equation
[F:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)C(C)C)C.[O:45]1[CH2:50][CH2:49][O:48][CH2:47][CH:46]1[C:51]1[C:59]2[S:58][C:57]([NH2:60])=[N:56][C:55]=2[C:54]([O:61][CH3:62])=[CH:53][CH:52]=1>C1COCC1.C(Cl)(Cl)Cl>[O:45]1[CH2:50][CH2:49][O:48][CH2:47][CH:46]1[C:51]1[C:59]2[S:58][C:57]([NH:60][C:4](=[O:6])[C:3]3[CH:7]=[CH:8][C:9]([F:11])=[CH:10][C:2]=3[F:1])=[N:56][C:55]=2[C:54]([O:61][CH3:62])=[CH:53][CH:52]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
From 2,4-difluorobenzoic acid, HATU and N-ethyldiisopropylamine in THF, then treatment with (+)-7-[1,4]dioxan-2-yl-4-methoxy-benzothiazol-2-ylamine. [α]D20=+19.4° (c=1.00, CHCl3), ES-MS m/e (%): 407 (M+H+, 100).
Sources & evidence
- ORD record
- ord-339daacaf3404ce1ac8355eace8b6b24
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06872833B2
Reaction notes
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