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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984450Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 9933605, compound

https://huagongshe.com/reaction/984450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant6-Amino-1-hexanolHCID 19960—
Reactant2,4-DichlorobenzenethiolHCID 70730—
ReactantPiperidin-4-olHCID 79341—
Reactant2-BromobenzenethiolHCID 80598—
Reactant3-Chloro-4-fluorobenzaldehydeHCID 593866—
ProductHCID 9933605HCID 9933605—

Reaction Steps

The title compound was prepared by the procedures described in Example 1 substituting 2,4-dichlorothiophenol with 2-bromothiophenol, 2-chlorobenzaldehyde with 3-chloro-4-fluoro-benzaldehyde, and 6-amino-1-hexanol with 4-hydroxypiperidine. 1H NMR (DMSO-d6, 300 MHz) δ 8.08 (d, J=1.7 Hz, 1H), 7.80 (dd, J=8.0, 1.5 Hz, 1H), 7.63 (dd, J=8.3, 1.9 Hz, 1H), 7.44 (ap dd, J=7.5, 1.4 Hz, 2H), 7.40 (ap d, J=3.7 Hz, 2H), 7.34 (dt, J=7.6, 1.8 Hz, 1H), 7.25 (dd, J=7.5, 1.7 Hz 1H), 7.05 (d, J=8.1 Hz, 1H), 4.16 (br s, 1H), 4.01 (m, 2H), 3.72 (m, 1H), 3.12 (m, 1H), 1.75 (m, 2H), 1.32 (m, 2H). HRMS calculated for C20H19N1O2S1Br1Cl1: 452.0087. Observed: 452.0076.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867203B2
Source datasetuspto-grants-2005_03
ORD IDord-ce3e1c7e07f44b08b2917e2b748dce4a
Source noteuspto-grants-2005_03