HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585037Generated: October 30, 2026
N-bromobutanimide → 6-Amino-5-bromo-1-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
https://huagongshe.com/reaction/585037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Amino-1-methyluracil | HCID 75520 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Amino-5-bromo-1-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione | HCID 255445 | 83% |
Reaction Steps
A mixture of 6-amino-1-methyluracil (14.0 g, 100 mmol), N-bromosuccinimide (21.0 g, 118 mmol), and dry DMF (250 mL) was heated at 80° C. for 3 h. The reaction mixture was evaporated in vacuo and the residue was slurried with ice-cold 50% aqueous ethanol (150 mL) and filtered. The resulting off-white solid was washed with ethanol, then ether and dried to yield 18.0 g 2a (83%). mp 274° C. dec; UV pH 1 λmax 276 nm; NMR δ (DMSO-d6) 3.26 (s, 3H, CH3), 7.02 (s, 2H, NH2), 10.89 (s, 1H, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06930101B1 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-3c524e69c53c4b8a83fb137e26ed6f5b |
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| Source note | uspto-grants-2005_08 |
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