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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098095Generated: October 30, 2026

8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine → HCID 178509328, compound

https://huagongshe.com/reaction/2098095

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidineHCID 68783490—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178509328HCID 178509328—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirring mixture of 8-chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine (60 mg, 0.285 mmol) in MeOH (10 mL) was added N-methylethyl 1,2-diamine (106 mg, 1.4 mmol). The resulting mixture was warmed to 60° C. for 1 hr. The reaction mixture was cooled to rt and then diluted with DCM. This mixture was then washed several times with a saturated NH4Cl solution. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure to give 5-chloro-3-(4H-1,2,4-triazol-3-yl)thiophen-2-amine. This amine was taken directly to the next coupling reaction without further purification. Retention time (min)=1.227, method [1], MS (ESI) 201.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-b601b6b4440c452a9f273182f0adf02a
Source noteuspto-grants-2013_05