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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098094Generated: October 31, 2026

Chlorosuccinimide → 8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine

https://huagongshe.com/reaction/2098094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantSodium BicarbonateHCID 516892—
ReactantThieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidineHCID 12226522—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetic AcidHCID 176—
Product8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidineHCID 68783490—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirring mixture of thieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine (123 mg, 0.7 mmol) in HOAc (1 mL) was added NCS (200 mg, 1.5 mmol), Pd(OAc)2 (48 mg, 0.21 mmol). The reaction mixture was stirred at 120° C. overnight. The reaction was neutralized with a saturated NaHCO3 solution and extracted with DCM. This product was purified via an isco column to give 8-chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine as the major product. Retention time (min)=1.663, method [1], MS (ESI) 211.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-ac6b56ded5f64c42ba865840db001697
Source noteuspto-grants-2013_05