HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Chlorosulfonyl)benzoic acid → 4-[4-(4-Oxo-piperidin-1-yl)-phenylsulfamoyl]-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Chlorosulfonyl)benzoic acid | HCID 82385 | — |
| Reactant | 1-(4-Amino-phenyl)-piperidin-4-one hydrochloride | HCID 22220240 | — |
| Product | 4-[4-(4-Oxo-piperidin-1-yl)-phenylsulfamoyl]-benzoic acid | HCID 22220295 | — |
Reaction Steps
The title compound was prepared from 4-(chlorosulfonyl)benzoic acid and 1-(4-amino-phenyl)-piperidine-4-one hydrochloride (which was obtained in Example 224) according to the procedure B of Example 225 as a pale grey solid; 1H NMR (300 MHz, DMSO-d6) δ 2.36 (t, J=6.0 Hz, 4H), 3.49 (t, J=6.0 Hz, 4H), 6.87 (d, J=9.3 Hz, 2H), 6.91 (d, J=9.3 Hz, 2H), 7.77 (d, J=8.1 Hz, 2H), 8.04 (d, J=8.1 Hz, 2H), 9.97 (s, 1H), 13.10 (brs, 1H); MS (ES) m/z: 374.9 (MH+); HRMS Calcd. for C18H19N2O5S(MH+): 375.1009. Found: 375.1009.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525202B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-b0c3181183c74090a94f5c2cc716cdf6 |
| Source note | uspto-grants-2003_02 |