HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lamotrigine → HCID 178511371, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lamotrigine | HCID 3878 | — |
| Reactant | (2,3-Dichlorophenyl)oxoacetonitrile | HCID 2735968 | — |
| Reactant | Benzoic acid, 2,3-dichloro-, anhydride with 2,3-dichlorobenzoic acid | HCID 20714991 | — |
| Reactant | HCID 178513185 | HCID 178513185 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 178511371 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06333198B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-52efb0685c5e40b7bbd602fafabebd66 |
| Source note | uspto-grants-2001_12 |