HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547380Generated: November 4, 2026
Diisopropylethylamine → N-[(4-fluorophenyl)methyl]-3-hydroxy-9-(methylamino)-4-oxo-pyrido[1,2-a]pyrimidine-2-carboxamide
https://huagongshe.com/reaction/547380
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(4-Fluorobenzyl)-3-hydroxy-9-(methylamino)-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidine-2-carboxamide | HCID 54709855 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | N-[(4-fluorophenyl)methyl]-3-hydroxy-9-(methylamino)-4-oxo-pyrido[1,2-a]pyrimidine-2-carboxamide | HCID 54730630 | — |
Reaction Steps
To a solution of N-(4-fluorobenzyl)-3-hydroxy-9-(methylamino)-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidine-2-carboxamide hydrotrifluoroacetate and diisopropylethylamine (4 eqs.) in o-xylene was added Pd(C) (10%). The suspension was stirred and heated to 156° C. for 7 hours. The suspension was left cooling to room temperature and the catalyst was filtered off. The catalyst was washed with methanol and dichloromethane and the filtrate and catalyst washes were combined and the combined organic solutions were concentrated to dryness. The product was purified by preparative RP-HPLC, using water (0.1% TFA) and acetonitrile (0.1% TFA) as eluants (column: C18). After lyophilization of the pooled product fractions the product was obtained 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-3b5b6a48ae244120bea923df66926ce7 |
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| Source note | uspto-grants-2011_05 |
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