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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10326Generated: October 25, 2026

Sodium hydride → 3-Amino-1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acid

https://huagongshe.com/reaction/10326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-Hydroxy-2,4-dinitrobenzenamineHCID 5743493—
Reactant1-Cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acidHCID 21979364—
Solvent1,4-dioxane N,N-dimethylformamideHCID 21712069—
Product3-Amino-1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acidHCID 2197900176.7%

Reaction Steps

A solution of 0.47 g (1.57 mmol) of 1-cyclopropyl-6-fluoro-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-7-thiosulfonic acid (Example 35) in 20 mL of dimethylformamide/dioxane (1:1) is treated portionwise with 0.08 g (2.0 mmol) of 60% sodium hydride/mineral oil. The reaction is stirred at room temperature for 1 hour and 0.32 g (1.6 mmol) of 2,4-dinitrophenylhydroxylamine is added all at once. After stirring at room temperature overnight, the dioxane is removed in vacuo and the residue is diluted to 100 mL with ice and water and stirred at 5° C. for 1 hour. The aqueous solution is extracted with ethyl acetate (3×50 mL) with the combined organic layers being washed with water, dried (MgSO4), filtered and evaporated in vacuo to give 0.4 g of the title compound, mp 167–169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094780B1
Source datasetuspto-grants-2006_08
ORD IDord-4df6972c6e4c48278a3fccf487f8d5a4
Source noteuspto-grants-2006_08