Cyclohexanecarboxylic acid → HCID 86594656, compound
Reaction equation
[CH:1]1([C:7]([OH:9])=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.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:43]1[CH2:48][CH2:47][O:46][CH2:45][CH:44]1[C:49]1[C:57]2[S:56][C:55]([NH2:58])=[N:54][C:53]=2[C:52]([O:59][CH3:60])=[CH:51][CH:50]=1>C1COCC1.C(Cl)(Cl)Cl>[O:43]1[CH2:48][CH2:47][O:46][CH2:45][CH:44]1[C:49]1[C:57]2[S:56][C:55]([NH:58][C:7]([CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)=[O:9])=[N:54][C:53]=2[C:52]([O:59][CH3:60])=[CH:51][CH:50]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
From cyclohexanecarboxylic acid, HATU and N-ethyldiisopropylamine in THF, then treatment with (+)-7-[1,4]dioxan-2-yl-4-methoxy-benzothiazol-2-ylamine. [α]D20=+19.2° (c=1.05, CHCl3), ES-MS m/e (%): 377 (M+H+, 100).
Sources & evidence
- ORD record
- ord-53403f9292b64d3ebbac9dc7bb351339
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06872833B2
Reaction notes
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