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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928591Generated: October 27, 2026

Cyclopropanecarboxamide → 4-Chloro-2-cyclopropyl-5-(2-methoxyphenyl)thieno[2,3-d]pyrimidine

https://huagongshe.com/reaction/928591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxamideHCID 80376—
ReactantEthyl 2-amino-4-(2-methoxyphenyl)thiophene-3-carboxylateHCID 16787922—
ReactantHCID 178479781HCID 178479781—
SolventDichloromethaneHCID 6344—
Product4-Chloro-2-cyclopropyl-5-(2-methoxyphenyl)thieno[2,3-d]pyrimidineHCID 8957936544.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl 2-amino-4-(2-methoxyphenyl)thiophene-3-carboxylate (1 g, 3.606 mmol), cyclopropanecarboxamide (0.3069 g, 3.606 mmol) and phosphorous (V) trichloride (0.6723 mL, 7.212 mmol) were combined and heated to 100° C. over the weekend in a Reactivial. The reaction mixture was diluted with DCM (25 mL), washed with water (2×25 mL), dried over Na2SO4 and concentrated at reduced pressure. The resulting residue was purified by flash chromatography, eluting with a gradient of petroleum ether to 50/50 petroleum ether/ethyl acetate to afford 4-chloro-2-cyclopropyl-5-(2-methoxyphenyl)thieno[2,3-d]pyrimidine (0.51 g). LCMS: purity 100%, RT=4.63 min, M+1=317.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290511B2
Source datasetuspto-grants-2016_03
ORD IDord-3bdd8f3589f940da98fcb4afe45af1b0
Source noteuspto-grants-2016_03