HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → 2,4,6-Trichloropyrimidine-5-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2,4,6-Trichloro-5-pyrimidinecarboxaldehyde | HCID 10932746 | — |
| Product | 2,4,6-Trichloropyrimidine-5-carbonyl chloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04464457 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-ab18ff4bc7e04237886fdcb6d9e1d6b4 |
| Source note | uspto-grants-1984_08 |