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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358118Generated: October 27, 2026

Sulfuryl chloride → 2,4,6-Trichloropyrimidine-5-carbonyl chloride

https://huagongshe.com/reaction/358118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant2,4,6-Trichloro-5-pyrimidinecarboxaldehydeHCID 10932746—
Product2,4,6-Trichloropyrimidine-5-carbonyl chlorideHCID 13264361—

Reaction Steps

In a first step, 2,4,6-trichloro-pyrimidine-5-carbaldehyde (I) is reacted with sulfuryl chloride to form 2,4,6-trichloropyrimidine-5-carboxylic acid chloride (II). The acyl chloride (II) is reacted, by a Friedel-Crafts-reaction, with an appropriately substituted benzene to form a 2,4,6-trichloro-pyrimidine-5-yl-aryl-ketone (III). Compound III is reacted with an aromatic amine in the presence of a tertiary amine to form a 2,4-dichloro-5-aroyl-6-arylamino-pyrimidine (IV).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464457
Source datasetuspto-grants-1984_08
ORD IDord-ab18ff4bc7e04237886fdcb6d9e1d6b4
Source noteuspto-grants-1984_08