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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237381Generated: October 26, 2026

Methanol → 2-Amino-4-(2,4-dichloro-5-hydroxyphenyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl amide

https://huagongshe.com/reaction/237381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron TrichlorideHCID 25135—
Reactant2-Amino-4-(5-benzyloxy-2,4-dichlorophenyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl amideHCID 44220101—
SolventDichloromethaneHCID 6344—
Product2-Amino-4-(2,4-dichloro-5-hydroxyphenyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl amideHCID 44220298—

Reaction Steps

Boron trichloride solution (1M in dichloromethane) was added to a suspension of 2-Amino-4-(5-benzyloxy-2,4-dichlorophenyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl amide in dichloromethane, at −78° C. under a nitrogen atmosphere. The suspension was stirred for ˜3 hrs at room temperature. The suspension was cooled in ice and methanol added, the resulting mixture was stirred for ˜1 hr. and concentrated to a yellow green solid. The solids were suspended in aqueous sodium acetate (10%) and extracted with ethyl acetate. The extracts were washed with water and saturated aqueous sodium chloride solution. The solution was dried over anhydrous sodium sulphate and concentrated to a pale brown solid, washed with hexane dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642594B2
Source datasetuspto-grants-2014_02
ORD IDord-c119329839b14a3ba98f6cdd0a891479
Source noteuspto-grants-2014_02