(Oxan-4-yl)methanesulfonyl chloride → 4-(Acetylthiomethyl)tetrahydropyran
Reaction equation
Cl[S:2]([CH2:5][CH:6]1[CH2:11][CH2:10][O:9][CH2:8][CH2:7]1)(=O)=O.[CH2:12]([O:19]C(C1(CS(N2CCN(C3C=CC(F)=CC=3)CC2)(=O)=O)CCOCC1)=O)[C:13]1C=CC=CC=1.FC1C=CC(N2CCN(S(CC3(C(O)=O)CCOCC3)(=O)=O)CC2)=CC=1>>[C:12]([S:2][CH2:5][CH:6]1[CH2:11][CH2:10][O:9][CH2:8][CH2:7]1)(=[O:19])[CH3:13]Participants
4
Reactant 3
Product 1
Procedure
MS (ESI): 331 (MNa+); 4-(chlorosulfonylmethyl)tetrahydropyran-4-(carboxylic acid benzyl ester): MS (ESI): 354 (MNa+); 4-[4-(4-fluorophenyl)piperazine-1-sulfonylmethyl]tetrahydropyran-4-carboxylic acid benzyl ester: MS (ESI): 477 (MH+), 499 (MNa+); 4-[4-(4-fluorophenyl)piperazine-1-sulfonylmethyl]tetrahydropyran-4-carboxylic acid: MS (ESI): 387 (MH+), 409 (MNa+).
Sources & evidence
- ORD record
- ord-4455bc473f8b403f89529abfba0176da
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07342020B2
Reaction notes
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