HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906695Generated: October 26, 2026
Sodium Hydroxide → 2-chloro-N-(4,6-dimethoxy-5-pyrimidinyl)-N-(1-(1-pyrazolyl)ethyl)acetamide
https://huagongshe.com/reaction/1906695
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(4,6-dimethoxypyrimidin-5-yl)chloroacetamide | HCID 15585336 | — |
| Reactant | N-(1-chloroethyl)pyrazole hydrochloride | HCID 20210169 | — |
| Catalyst | Benzyltributylammonium chloride | HCID 159952 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-chloro-N-(4,6-dimethoxy-5-pyrimidinyl)-N-(1-(1-pyrazolyl)ethyl)acetamide | HCID 13825097 | 37.9% |
Reaction Steps
In a 500 ml eggplant-shaped flask equipped with a stirrer, 17.4 g (75.1 mmoles) of 2-chloro-N-(4,6-dimethoxy-5-pyrimidinyl)acetamide was dissolved in 300 ml of dichloromethane, and 5.22 g of benzyl tributyl ammonium chloride was added. Under ice cooling, 41.5 ml of a 50% aqueous solution of sodium hydroxide was added to the mixture with stirring. Thereafter, a solution of 13.8 g (82.6 mmoles) of N-(1-chloroethyl)pyrazole hydrochloride in 70 ml of dichloromethane was added dropwise over about 30 minutes. The mixture was stirred further at room temperature for 2 hours. The reaction mixture was washed with water, dried and concentrated. The resulting solid was recrystallized from isopropanol to give 9.26 g of 2-chloro-N-(4,6-dimethoxy-5-pyrimidinyl)-N-(1-(1-pyrazolyl)ethyl)acetamide as a pale yelllow solid which had the following properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04654074 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-10b58830dafd48c0b6e449fd8a9669a0 |
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| Source note | uspto-grants-1987_03 |
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