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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426260Generated: November 2, 2026

Tetrahydrofuran → 9-[dimethylsulfamoyl(methyl)amino]-N-[(4-fluorophenyl)methyl]-3-hydroxy-4-oxo-6,7,8,9-tetrahydropyrido[1,2-a]pyrimidine-2-carboxamide

https://huagongshe.com/reaction/2426260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantDimethylsulphamoyl chlorideHCID 83372—
ReactantN-(4-Fluorobenzyl)-3-hydroxy-9-(methylamino)-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidine-2-carboxamideHCID 54709855—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product9-[dimethylsulfamoyl(methyl)amino]-N-[(4-fluorophenyl)methyl]-3-hydroxy-4-oxo-6,7,8,9-tetrahydropyrido[1,2-a]pyrimidine-2-carboxamideHCID 54709838—

Reaction Steps

To a solution of crude compound obtained in Step 3 in a 2:1 mixture of tetrahydrofuran and 2 M aq. sodium hydroxide was added N,N-dimethylsulfamoyl chloride (4.6 eq.). The mixture was stirred at room temperature for 16 h. The mixture was concentrated under reduced pressure and the product was isolated by preparative RP-HPLC, using water (0.1% TFA) and acetonitrile (0.1% TFA) as eluents (column: C18). The pooled product fractions were lyophilized to afford the title compound as a fluffy, slightly pink material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968553B2
Source datasetuspto-grants-2011_06
ORD IDord-477f6f3a20be4b659581527f3633333a
Source noteuspto-grants-2011_06