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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061393Generated: October 25, 2026

1-Butanesulfonic acid → HCID 69655077, compound

https://huagongshe.com/reaction/1061393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Butanesulfonic acidHCID 49935—
ReactantHCID 69655051HCID 69655051—
ReactantN-[4-(4-Oxo-1-piperidinyl)phenyl]-1-butanesulfonamideHCID 86584570—
ProductHCID 69655077HCID 69655077—

Reaction Steps

The title compound was prepared from butane-1-sulfonic acid ]4-(4-oxo-piperidine-1-yl)-phenyl]-amide (which was obtained in Example 228) and 5-(3-amino-(2S)-2-hydroxy-propoxy)-8-hydroxy-3,4-dihydro-1H-quinolin-2-one (which was obtained in Example 12) according to the procedure of Example 278 as a white solid; 1H NMR (300 MHz, DMSO-d6) δ 0.82 (t, J=7.3 Hz, 3H), 1.20-1.40 (m, 4H), 1.50-1.70 (m, 2H), 1.80-1.95 (m, 2H), 2.39 (t, J=7.3 Hz, 2H), 2.50-2.80 (m, 5H), 2.85 (t, J=7.3 Hz, 2H), 2.85-3.00 (m, 2H), 3.45-3.60 (m, 2H), 3.75-3.85 (m, 3H), 6.44 (d, J=8.7 Hz, 1H), 6.60 (d, J=8.7 Hz, 1H), 6.89 (d, J=9.0 Hz, 2H), 7.04 (d, J=9.0 Hz, 2H), 8.74 (s, 1H); MS (ES) m/z: 546.9 (MH+); HRMS Calcd. for C27H39N4O6S(MH+): 547.2590. Found: 547.2583.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-be1fd317e0344e5b8ce7a8b8e2f246e4
Source noteuspto-grants-2003_02