HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962202Generated: November 1, 2026
N,N-Dimethylaniline → 4-Chloro-6-cyclopentylpyrimidin-2-amine
https://huagongshe.com/reaction/1962202
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Amino-6-cyclopentylpyrimidin-4-OL | HCID 135493693 | — |
| Catalyst | Tetraethylammonium Chloride | HCID 5946 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Chloro-6-cyclopentylpyrimidin-2-amine | HCID 21846367 | 120.5% |
Reaction Steps
A suspension of 2-amino-6-cyclopentyl-3H-pyrimidin-4-one (1.52 g, 8.4 mmol), tetraethyl ammonium chloride (2.8 g 16.9 mmol) and dimethylaniline (1.1 mL, 8.4 mmol) in acetonitrile (16 mL) was treated with phosphorous oxychloride (4.7 mL, 51 mmol) and heated at 110° C. for 20 min. The resulting solution was cooled to rt and concentrated to minimum volume then diluted with CHCl3 and ice and stirred for 30 min. The layers were separated and the organic layer was washed with water (3×50 mL) and 5% NaHCO3, dried, and concentrated to yield 2.0 g of crude product that was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415366B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-2fc4d758c5ba406e9cd54777b5e418f4 |
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| Source note | uspto-grants-2013_04 |
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