HCID 20505839, compound → HCID 20505992, compound
Reaction equation
[CH2:1]([N:3]([CH2:17][CH3:18])[S:4]([C:7]1[CH:8]=[CH:9][CH:10]=[C:11]([C:15]=1[Cl:16])[C:12]([OH:14])=[O:13])(=[O:6])=[O:5])[CH3:2].N1(S(C2C=CC=C(C=2F)C(O)=O)(=O)=[O:26])CCCCC1.C(N(CCC)S(C1C=CC=C(C=1F)C(O)=O)(=O)=O)CC.C1(NS(C2C=CC=C(C=2Br)C(O)=O)(=O)=O)C=CC=CC=1.C[C@H]1C[C@@H](C)CN(S(C2C=CC=C(C=2Br)C(O)=O)(=O)=O)C1.CN(C)S(C1C=CC=C(C=1Br)C(O)=O)(=O)=O.N1(S(C2C=CC=C(C=2Br)C(O)=O)(=O)=O)CCCCC1.CC1CC(C)CCN1S(C1C=CC=C(C=1C)C(O)=O)(=O)=O.CC1(C)CCN(S(C2C=CC=C(C=2C)C(O)=O)(=O)=O)CC1.ClC1C(Cl)=CC=CC=1CNS(C1C=CC=C(C=1C)C(O)=O)(=O)=O.C(N(CCCC)S(C1C=CC=C(C=1C)C(O)=O)(=O)=O)CCC.O1CCN(S(C2C=CC=C(C=2C)C(O)=O)(=O)=O)CC1>>[O:26]1[CH2:2][CH2:1][N:3]([S:4]([C:7]2[CH:8]=[CH:9][CH:10]=[C:11]([C:15]=2[Cl:16])[C:12]([OH:14])=[O:13])(=[O:5])=[O:6])[CH2:17][CH2:18]1Participants
Reactant 12
Product 1
Procedure
5-diethylaminosulfonyl-6-chlorobenzoic acid; 5-(2-p-chlorophenethylaminosulfonyl)-6-chlorobenzoic acid; 5-hexamethyleneiminosulfonyl-6-fluorobenzoic acid; 5-piperidinosulfonyl-6-fluorobenzoic acid; 5-di-n-propylaminosulfonyl-6-fluorobenzoic acid; 5-(2-p-bromophenethylaminosulfonyl)-6-fluorobenzoic acid; 5-phenylaminosulfonyl-6-bromobenzoic acid; 5-(cis-3,5-dimethylpiperidinosulfonyl)-6-bromobenzoic acid; 5-dimethylaminosulfonyl-6-bromobenzoic acid; 5-hexamethyleneiminosulfonyl-6-bromobenzoic acid; 5-piperidinosulfonyl-6-bromobenzoic acid; 5-(2,4-dimethylpiperidinosulfonyl)-6-methylbenzoic acid; 5-(4,4-dimethylpiperidinosulfonyl)-6-methylbenzoic acid; 5-(2-p-chlorophenethylaminosulfonyl)-6-methylbenzoic acid; 5-(2,3-dichlorobenzylaminosulfonyl)-6-methylbenzoic acid; 5-di-n-butylaminosulfonyl-6-methylbenzoic acid; and 5-morpholinosulfonyl-6-methylbenzoic acid.
Sources & evidence
- ORD record
- ord-56678dc36f2042f2a20b70c92c1e6624
- Source dataset
- uspto-grants-1983_03
- Patent number
- US04377521
Reaction notes
Loading…