HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824735Generated: October 27, 2026
2,4-Dimethoxy-3-iodopyrimidine → (s)-n-Methyl-n-(tert-butoxycarbonyl)-5-(2,4-dimethoxy-5-pyrimidinyl)-4-penten-2-amine
https://huagongshe.com/reaction/1824735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dimethoxy-3-iodopyrimidine | HCID 22144491 | — |
| Reactant | (S)-tert-butyl methyl(pent-4-en-2-yl)carbamate | HCID 54671306 | — |
| Reactant | HCID 178484883 | HCID 178484883 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | (s)-n-Methyl-n-(tert-butoxycarbonyl)-5-(2,4-dimethoxy-5-pyrimidinyl)-4-penten-2-amine | HCID 68597348 | — |
Reaction Steps
Scheme I shows the synthesis of (S)-N-methyl-5-(2,4-dihydroxy-5-pyrimidinyl)-4-penten-2-amine. In this synthesis, the previously described (S)-N-methyl-N-(tert-butoxycarbonyl)-4-penten-2-amine is subjected to Heck-type coupling conditions by reaction with a 2,4-dimethoxy-3-iodopyrimidine in the presence of a palladium catalyst to form (S)-N-methyl-N-(tert-butoxycarbonyl)-5-(2,4-dimethoxy-5-pyrimidinyl)-4-penten-2-amine. The methoxy groups can be converted to hydroxy groups, concurrent with the cleavage of the amine protecting group, by reaction with trimethylsilyl iodide in methanol/dichloromethane to yield the desired N-methyl-5-(2,4-dihydroxy-5-pyrimidinyl)-4-penten-2-amine compound as a hydroiodide salt. Alternately, the tert-butoxycarbonyl protecting group can be selectively removed by trifluoroacetic acid, as described previously, to give the (S)-N-methyl-5-(2,4-dimethoxy-5-pyrimidinyl)-4-penten-2-amine. Cleavage of the methyl ethers using 48% HBr then provides (S)-N-methyl-5-(2,4-dihydroxy-5-pyrimidinyl)-4-penten-2-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045538B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-2b912c6f3c5d40369c0701a2a49bac8a |
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| Source note | uspto-grants-2006_05 |
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