HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41367Generated: October 28, 2026
Hydrochloric Acid → 4-((4-Amino-5,6-dichloropyrimidin-2-yl)amino)benzonitrile
https://huagongshe.com/reaction/41367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | 2,5,6-Trichloropyrimidin-4-amine | HCID 15850196 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-((4-Amino-5,6-dichloropyrimidin-2-yl)amino)benzonitrile | HCID 22170098 | 6.8% |
Reaction Steps
To a flask under Argon was added 4-amino-2,5,6-trichloropyrimidine (0.08564 mol), 4-amino-benzonitrile (0.1071 mol), 1-methyl-2-pyrrolidinone (17 ml) and HCl in diethylether (1M; 85.6 ml). The mixture was placed in an oil bath at 130° C. under a stream of nitrogen until the ether was gone. An additional 10 ml of 1-methyl-2-pyrrolidinone was added. The mixture was heated at 145° C. for 16 hours under argon. 1,4-Dioxane was added. The mixture was refluxed, cooled, then filtered. The filtrate was evaporated. The residue was dissolved in CH2Cl2, washed with 1 N NaOH, then filtered. The solid was dissolved in 2-propanone, evaporated onto silica gel, and chromatographed using 1-3% 2-propanone in hexane as eluent. The pure fractions were collected and the solvent was evaporated, yielding 1.63 g (6.8%) of 4-[(4-amino-5,6-dichloro-2-pyrimidinyl)amino]benzonitrile (interm. 12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530655B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-52d15fc4d6fc4139af8d6f37a462d641 |
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| Source note | uspto-grants-2013_09 |
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