HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591222Generated: October 30, 2026
3-Amino-2-imino-6-methyl-2,3-dihydropyrimidin-4(1H)-one → HCID 178429168, compound
https://huagongshe.com/reaction/591222
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Amino-2-imino-6-methyl-2,3-dihydropyrimidin-4(1H)-one | HCID 913175 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 2,2-difluoropropanoate | HCID 2761188 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178429168 | HCID 178429168 | — |
Reaction Steps
Intermediate 1 was added to a stirring solution of NaOEt prepared from sodium (FLUKA, 3.28 g, 143 mmol) and ethanol (150 ml) and the mixture was heated at 80° C. for 30 minutes. The reaction mixture was cooled down to room temperature and ethyl 2,2-difluoropropanoate (FLUOROCHEM, 11.83 g, 86 mmol) was added. The mixture was stirred at room temperature for 30 min before being heated to 80° C. for 1.5 h. The reaction mixture was concentrated to dryness and water (200 mL) was added. The reaction mixture pH was adjusted to 4 by addition of 2N HCl solution while a white solid precipitated. The solid was filtered, washed with water and dried under vacuum to afford Intermediate 2. The mother liquors were extracted with DCM (5×35 mL) and the combined organic layers were dried over Na2SO4, filtered, and concentrated under vacuum to give more Intermediate 2 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238653B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-287c7d10561a4e5a970b756f1d7369e5 |
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| Source note | uspto-grants-2016_01 |
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