HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113178Generated: October 29, 2026
Guanidine Hydrochloride → HCID 178459352, compound
https://huagongshe.com/reaction/2113178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | Propan-2-yl 4-methyl-3-oxopentanoate | HCID 57643949 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178459352 | HCID 178459352 | 67% |
Reaction Steps
Guanidine hydrochloride (12.1 g), 4-Fluorobenzaldehyde (7.0 g), isopropyl 4-methyl-3-oxo-pentanoate (8.9 g) and DMF (150 ml) were charged to a vessel equipped with a condenser and connected to a nitrogen line. The resultant mixture was stirred until a clear solution was obtained. Potassium carbonate (17.5 g) was charged and the mixture heated to 70° C. for 3 hours. The reaction mixture was cooled to ambient temperature, filtered, and the solvents removed by evaporation under reduced pressure. The resultant oil was triturated in water at 80° C. and cooled to give a slurry that was filtered and dried to give isopropyl 2-amino-4-(4-fluorophenyl)-6-isopropyl-1,6-dihydropyrimidine-5-carboxylate in 67% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524955B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-2c90436d55d2455a934abbd4a3ca0673 |
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| Source note | uspto-grants-2009_04 |
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