Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Methanesulfonyl)acetyl chloride | HCID 21288095 | — |
| Reactant | N-[(4-fluorophenyl)methyl]-3-hydroxy-9-(methylamino)-4-oxo-pyrido[1,2-a]pyrimidine-2-carboxamide | HCID 54730630 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57855384 | HCID 57855384 | — |
Reaction Steps
N-(4-fluorobenzyl)-3-hydroxy-9-(methylamino)-4-oxo-4H-pyrido[1,2-a]pyrimidine-2-carboxamide was dissolved in dichloromethane. Methylsulfonylacetyl chloride (1.2 eqs.) and triethylamine (2 eqs.) were added and the solution was stirred at room temperature. After 5 hours a further 2 eqs. of methylsulfonylacetyl chloride and 2 eqs. of triethylamine were added. The solvent was removed under vacuum and the residue was suspended in methano/0.1 M NaOH. The suspension was sonicated for 2 minutes and left stirring at room temperature for 30 minutes. The product was purified by preparative RP-HPLC, using water (0.1% TFA) and acetonitrile (0.1% TFA) as eluants (column: C18). The product was obtained after lyophilization of the pooled product fractions as bright yellow fluffy material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07939537B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-57e924651afc447291c5125d851a582b |
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| Source note | uspto-grants-2011_05 |
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