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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270885Generated: November 1, 2026

Lamotrigine → HCID 178511371, compound

https://huagongshe.com/reaction/2270885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLamotrigineHCID 3878—
Reactant(2,3-Dichlorophenyl)oxoacetonitrileHCID 2735968—
ReactantBenzoic acid, 2,3-dichloro-, anhydride with 2,3-dichlorobenzoic acidHCID 20714991—
ReactantHCID 178513185HCID 178513185—
SolventSulfuric AcidHCID 1118—
ProductHCID 178511371HCID 178511371—

Reaction Steps

The synthesis of lamotrigine is illustrated in Reference Example 1. 2,3-Dichlorobenzoyl cyanide, which is intermediate 1.4 in that synthesis, may contain up to 10% of 2,3-dichlorobenzoic anhydride as a contaminant. When the 2,3-dichlorobenzoyl cyanide is treated with a solution of aminoguanidine bicarbonate in sulphuric acid, which is step (d) in Reference Example 1, the adduct (Z)-2-(2,3-dichlorophenyl)-2-(guanidinoimino)acetonitrile (intermediate 1.5) is produced. The anhydride contaminant can then react with the latter adduct to form (Z)-2-(2,3-dichlorophenyl)-2-[N′-(2,3-dichlorobenzoyl)guanidinoimino]acetonitrile, which is the direct precursor to compound B. Cyclisation of the precursor in propan-1-ol under reflux yields compound B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333198B1
Source datasetuspto-grants-2001_12
ORD IDord-52efb0685c5e40b7bbd602fafabebd66
Source noteuspto-grants-2001_12