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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 5-Chloro-2-(methylsulfanyl)pyrimidine-4-carboxylic acid | HCID 725711 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2-(methylthio)pyrimidine-4-carbohydrazide | HCID 43244768 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858785B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-ebd15e7726f34cc9a7db4ba5a871c6a2 |
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| Source note | uspto-grants-2010_12 |
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