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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984454Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 10370763, compound

https://huagongshe.com/reaction/984454

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant6-Amino-1-hexanolHCID 19960—
Reactant2,4-DichlorobenzenethiolHCID 70730—
Reactant2-BromobenzenethiolHCID 80598—
Reactant1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 88638—
Reactant3-Chloro-4-fluorobenzaldehydeHCID 593866—
ProductHCID 10370763HCID 10370763—

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-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidine. 1H NMR (DMSO-d6, 300 MHz) δ 8.14 (d, J=1.5 Hz, 1H), 7.80 (dd, J=7.9, 1.3 Hz, 1H), 7.67 (dd, J=8.1, 1.8 Hz, 1H), 7.48 (ap s, 2H), 7.44 (dt, J=7.5, 1.2, 1H), 7.34 (dt, J=7.6, 1.6, 1H), 7.26 (dd, J=7.7, 1.8 Hz, 1H), 7.22 (m, 1H), 7.06 (d, J=8.1, 1H), 6.97 (ap d, J=2.6, 3H), 4.64 (m, 1H), 4.48 (m, 2H), 2.79 (m, 2H), 2.29 (m, 2H), 1.78 (in, 2H). HRMS calculated for C27H23N3O2S1Br1Cl1: 568.0461. Observed: 568.0477.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867203B2
Source datasetuspto-grants-2005_03
ORD IDord-8e1659d0933b4156aaf7ee2c3c49d1df
Source noteuspto-grants-2005_03