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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246791Generated: October 25, 2026

4-Chloro-2-fluorobenzoyl chloride → HCID 21905770, compound

https://huagongshe.com/reaction/1246791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluorobenzoyl chlorideHCID 2773601—
Reactant6-Chloro-N4-(4-chlorophenyl)pyrimidine-4,5-diamineHCID 16726311—
SolventEthanolHCID 702—
SolventPyridineHCID 1049—
ProductHCID 21905770HCID 21905770—

Reaction Steps

6-Chloro-N4-(4-chlorophenyl)-pyrimidine-4,5-diamine I-(1A-1)a (6.6 g, 26 mmol) in pyridine (30 ml) was cooled to 0° C. and to it was added 4-chloro-2-fluorobenzoyl chloride (5 g, 26 mmol). The reaction was then allowed to warm to ambient temperature overnight. The heterogeneous reaction was diluted with ethanol (50 ml) and the resulting solid collected by filtration. The solids were slurried in toluene, which was then removed under reduced pressure to remove residual ethanol. The solid was slurried in diethyl ether and then collected by filtration to give I-(7A-91)a (8.3 g, 78%): +ACPI MS (M+1) 409.0; 1H NMR (400 MHz, CD3OD) δ 10.60 (s, 1H), 10.10 (s, 1H), 9.19 (s, 1H), 8.74 (t, J=8.1 Hz, 1H), 8.46–8.40 (m, 3H), 8.28 (dd, J=8.7, 2.1 Hz, 1H), 8.20 (d, J=8.7 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129239B2
Source datasetuspto-grants-2006_10
ORD IDord-1800146ac7c349e69101ea3ed85714e4
Source noteuspto-grants-2006_10