HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071047Generated: October 31, 2026
Guanidine Hydrochloride → HCID 68671207, compound
https://huagongshe.com/reaction/2071047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-methoxy-5-methylhexane-2,4-dione | HCID 10012154 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68671207 | HCID 68671207 | 39.1% |
Reaction Steps
To a stirred solution of 1-methoxy-5-methylhexane-2,4-dione (1.08 g, 6.8 mmol) in EtOH (15 mL) was added guanidine hydrochloride (1.3 g, 13.7 mmol). 5 min later, a solution of Na2CO3 (1.45 g, 13.7 mmol) in H2O was added and the resulting mixture was heated to reflux for 20 h. The reaction was cooled to room temperature and the solvent was removed. The residue was dissolved in EtOAc (20 mL) and H2O (20 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2×20 mL). The combined organic layer was washed with brine, dried with Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (50% EtOAc in hexanes) to provide 4-isopropyl-6-(methoxymethyl)pyrimidin-2-amine (482 mg, 39%). 1H NMR (CDCl3): d 6.43 (s, 1H), 6.11 (s, 2H), 4.16 (s, 2H), 3.26 (s, 3H), 2.56-2.66 (m, 1H), 1.03 (d, J=6.9 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299267B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-948049866d2b44f7bf7716d4d6962a76 |
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| Source note | uspto-grants-2012_10 |
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