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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267421Generated: October 28, 2026

Hydrazine hydrate (1:1) → 5-Chloro-2-(methylthio)pyrimidine-4-carbohydrazide

https://huagongshe.com/reaction/2267421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant5-Chloro-2-(methylsulfanyl)pyrimidine-4-carboxylic acidHCID 725711—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-(methylthio)pyrimidine-4-carbohydrazideHCID 4324476858%

Reaction Steps

5-Chloro-2-(methylthio)pyrimidine-4-carboxylic acid (4.0 g, 19.6 mmol) and 1,1-carbonyl diimidazole (6.35 g, 39.2 mmol) were dissolved in 80 mL THF and stirred at room temperature. After 3 h, the solution was cooled in an ice bath and hydrazine hydrate (1.90 mL, 39.2 mmol) was added in one quick portion. The solution was allowed to stir for 5 h, gradually warming to room temperature. The reaction mixture was diluted with excess H2O and extracted with EtOAc several times. These organics were combined and washed with 2 N HCl. The combined aqueous layers were then basified carefully with 5 N NaOH, and extracted once again with EtOAc. This second set of organic layers was combined, dried over magnesium sulfate and concentrated under vacuum to give 2.46 g (58% yield) of product as a white solid. MS (M+H)+ 219.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-ebd15e7726f34cc9a7db4ba5a871c6a2
Source noteuspto-grants-2010_12