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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167142Generated: October 30, 2026

Dimethylformamide → (3-Propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene)methylamine

https://huagongshe.com/reaction/1167142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene amineHCID 22995819—
Product(3-Propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene)methylamineHCID 69986416—

Reaction Steps

In a sulfonation flask 4.5 g (0.018 mol) 3-propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene amine, 5.1 g (0.036 mol) CH3I, 5.0 g (0.036 mol) powdered potassium carbonate and 80 ml of absolute DMF are stirred for 4 hours at an internal temperature of 90-100° C. Then the solvent is distilled off in vacuum, the residue taken up in ethylacetate and the organic phase twice washed with water. After drying the organic phase over Na2SO4 the ethylacetate is distilled off in a water jet vacuum and the residue purified by column chromatography over silica gel (eluant: hexane/ethylacetate 1:6). Yield: 4.4 g of (3-propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene)methylamine in the form of a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617330B2
Source datasetuspto-grants-2003_09
ORD IDord-ad9813d6fb9a49c299a7c49a782ff21a
Source noteuspto-grants-2003_09