HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831992Generated: October 25, 2026
4-Amino-2-methyl-5-pyrimidinemethanamine → HCID 54724214, compound
https://huagongshe.com/reaction/1831992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Amino-2-methyl-5-pyrimidinemethanamine | HCID 66762 | — |
| Reactant | 4-Hydroxy-6-methyl-2-pyrone | HCID 54675757 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54724214 | HCID 54724214 | 58.6% |
Reaction Steps
A mixture of 4-hydroxy-6-methyl-2-pyrone (0.9 g, 0.007 mol) and 4-amino-5-aminomethyl-2-methylpyrimidine (1.0 g, 0.007 mol) in water (10.0 ml) was heated at 100° C. for 1 h under argon atmosphere. The reaction mixture was cooled, and filtered the yellow precipitate. It was washed successively with cold water, ethanol, and dried in vacuo to afford the title compound (1.01 g, 51%) as a pale yellow powder: 1H NMR (DMSO-d6/400 MHz) δ 7.62 (s, 1H), 7.04 (s, 1H), 5.83 (d, 1H, J=2.0 Hz), 5.58 (d, 1H, J=2.0 Hz), 4.92 (s, 2H), 2.24 (s, 3H), and 2.22 (s, 3H); ES-HRMS m/z 325.0304 (M+H C12H14N4O2Br requires 325.0295). Step 2 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-hydroxy-6-methylpyridin-2(1H)-one
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067540B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-3dba739c2a4d4cffbeddd87551f97052 |
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| Source note | uspto-grants-2006_06 |
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