HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729642Generated: October 30, 2026
Water → Methyl 2-(3-fluorophenyl)pyrimidine-5-carboxylate
https://huagongshe.com/reaction/729642
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-fluorobenzenecarboximidamide | HCID 3639345 | — |
| Product | Methyl 2-(3-fluorophenyl)pyrimidine-5-carboxylate | HCID 45073367 | 59% |
Reaction Steps
To a solution of methyl 3,3-dimethoxypropionate (304 g, 2.05 mol) in dimethoxyethane (1.5 L) was added methyl formate (580 g, 9.44 mol). Sodium hydride (98.5 g, 60% suspension in mineral oil, 2.46 mol) was added portion-wise and the mixture was stirred at 50° C. for 5 hours and then at room temperature overnight. Diethyl ether (1.5 L) was added and the reaction was filtered under an atmosphere of nitrogen. The solid residue was washed with diethyl ether (300 mL×2) and dried to give 200 g (68.9%) of [methyl-2-(dimethoxymethyl)-3-(hydroxyl-kappaO)acrylatato]sodium. A mixture of this compound (63.5 g, 0.32 mol), 3-fluorobenzenecarboximidamide (38 g, 0.27 mol) and dimethylformamide (400 mL) was heated at 100° C. for 2 h. After this time the reaction was cooled to room temperature and water (400 mL) was added. The reaction was filtered and the residue was washed with water (100 mL×2) and dried to give 37 g (yield 59%) of methyl 2-(3-fluorophenyl)pyrimidine-5-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582643B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-01ba52efda9545e78887a70d2b4602f8 |
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| Source note | uspto-grants-2009_09 |
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