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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984448Generated: October 30, 2026

2-Chlorobenzaldehyde → HCID 9912394, compound

https://huagongshe.com/reaction/984448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant6-Amino-1-hexanolHCID 19960—
Reactant2,4-DichlorobenzenethiolHCID 70730—
Reactant2-BromobenzenethiolHCID 80598—
ReactantPiperidin-3-ylmethanolHCID 107308—
Reactant3-Chloro-4-fluorobenzaldehydeHCID 593866—
ProductHCID 9912394HCID 9912394—

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 3-hydroxymethylpiperidine. 1H NMR (DMSO-d6, 300 MHz) δ 8.07 (d, J=17.7 Hz, 1H), 7.80 (d, J=7.7 Hz, 1H), 7.63 (br d, J=7.7 Hz, 1H), 7.44 (d, J=7.0 Hz, 1H), 7.40 (br s, 2H), 7.35 (m, 1H), 7.25 (dd 7.7, 1.5, 1H), 7.06 (dd, J=8.1, 2.9, 1H), 4.57 (m, 1H), 4.45 (m, 1H), 4.16 (br m, 2H), 1.2-1.8 (m, 8H). HRMS calculated for C21H21N1O2S1Br1Cl1: 466.0243. Observed: 466.0247.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867203B2
Source datasetuspto-grants-2005_03
ORD IDord-5ceab78143a84d52b194036a71349cd2
Source noteuspto-grants-2005_03