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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921721Generated: October 29, 2026

Methyl chloroacetate → Methyl 2-((5-amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetate

https://huagongshe.com/reaction/1921721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroacetateHCID 7295—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178509206HCID 178509206—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-((5-amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetateHCID 59763691—

Reaction Steps

Methyl 2-chloroacetate (0.73 mL, 8.3 mmol) was added dropwise over 5 mins to a suspension of 5-amino-4-(1-cyclopropylnaphthalen-4-yl)-4H-1,2,4-triazole-3-thiol (2.24 g, 7.9 mmol) and potassium carbonate (1.21 g, 8.7 mmol) in DMF (40 mL) at room temperature. The reaction was stirred at room temperature for 24 h and slowly poured into a stirred ice-cold water solution. The tan precipitate was collected by vacuum filtration and dried under high vacuum at 50° C. for 16 h in the presence of P2O5 to yield methyl 2-(5-amino-4-(1-cyclopropylnaphthalen-4-yl)-4H-1,2,4-triazol-3-ylthio)acetate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173690B2
Source datasetuspto-grants-2012_05
ORD IDord-301d0d67937243d2a7c0acef29a7c946
Source noteuspto-grants-2012_05