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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76073Generated: November 1, 2026

Phosphorus oxychloride → (4-[4-(6-Chloro-pyridazin-3-yl)-phenyl]-cyclohexyl)-acetic acid ethyl ester

https://huagongshe.com/reaction/76073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 66615831HCID 66615831—
SolventTolueneHCID 1140—
Product(4-[4-(6-Chloro-pyridazin-3-yl)-phenyl]-cyclohexyl)-acetic acid ethyl esterHCID 86634692—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 50 Ml flask was charged with {4-[4-(6-oxo-1,6-dihydro-pyridazin-3-yl)-phenyl]-cyclohexyl}-acetic acid ethyl ester (0.76 g, 2.2 mmol, 1.0 equiv) in 20 Ml toluene followed by phosphorous oxychloride (0.62 Ml, 6.7 mmol, 3.0 equiv). The suspension was heated to 100° C., at which point a homogeneous solution ensued. The reaction was stirred overnight at 100° C., then cooled to room temperature. Removal of volatiles in vacuo afforded the title compound: 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.07-1.17 (m, 2H) 1.20 (t, J=7.07 Hz, 3H) 1.43-1.53 (m, 2H) 1.78-1.90 (m, 5H) 2.18 (d, J=6.57 Hz, 2H) 2.44-2.52 (m, 1H) 4.08 (q, J=7.07 Hz, 2H) 7.29 (d, J=8.34 Hz, 2H) 7.46 (d, J=9.09 Hz, 1H) 7.72 (d, J=9.09 Hz, 1H) 7.90 (d, J=8.59 Hz, 2H); (M+H)+359.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835451B2
Source datasetuspto-grants-2014_09
ORD IDord-90e058e3934a4cf49a7990ec6b7cd3cd
Source noteuspto-grants-2014_09