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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061399Generated: November 2, 2026

HCID 69654876, compound → HCID 69654705, compound

https://huagongshe.com/reaction/1061399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69654876HCID 69654876—
ReactantN-[4-(4-Oxo-1-piperidinyl)phenyl]-1-butanesulfonamideHCID 86584570—
ProductHCID 69654705HCID 69654705—

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 N-[5-((2S)-3-amino-2-hydroxy-propoxy)-2-hydroxy-phenyl]-benzenesulfonamide (which was obtained in Example 21) according to the procedure of Example 278 as an off-white solid; 1H NMR (300 MHz, DMSO-d6) δ 0.83 (t, J=7.3 Hz, 3H), 1.20-1.40 (m, 4H), 1.55-1.70 (m, 2H), 1.80-1.95 (m, 2H), 2.50-2.80 (m, 5H), 2.92 (t, J=7.6 Hz, 2H), 3.50-3.90 (m, 5H), 6.39 (d, J=8.7, 2.9 Hz, 1H), 6.57 (d, J=8.7 Hz, 1H), 6.72 (d, J=2.9 Hz, 1H), 6.90 (d, J=9.0 Hz, 2H), 7.05 (d, J=9.0 Hz, 2H), 7.40-7.60 (m, 3H), 7.74 (d, J=7.7 Hz, 2H); MS (ES) m/z: 633.1 (MH+); HRMS Calcd. for C30H41N4O7S2 (MH+): 633.2411. Found: 633.2409.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-7bdeb049aa1648389f5d8fc5f3bb913a
Source noteuspto-grants-2003_02