Diisopropylethylamine → HCID 22507720, compound
Reaction equation
[F:1][C:2]1[CH:10]=[C:9]([O:11][CH3:12])[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:46]1[CH2:51][CH2:50][O:49][CH2:48][CH:47]1[C:52]1[C:60]2[S:59][C:58]([NH2:61])=[N:57][C:56]=2[C:55]([O:62][CH3:63])=[CH:54][CH:53]=1>C1COCC1.C(Cl)(Cl)Cl>[O:46]1[CH2:51][CH2:50][O:49][CH2:48][CH:47]1[C:52]1[C:60]2[S:59][C:58]([NH:61][C:4](=[O:6])[C:3]3[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:2]=3[F:1])=[N:57][C:56]=2[C:55]([O:62][CH3:63])=[CH:54][CH:53]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
From 2-fluoro-4-methoxybenzoic 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=1.02, CHCl3), ES-MS m/e (%): 419 (M+H+, 100).
Sources & evidence
- ORD record
- ord-ee45c25b779641dd8748bd2a411cb1ac
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06872833B2
Reaction notes
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