Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937403Generated: October 26, 2026

Oxalyl chloride → 4-(3-Ethynyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic Acid Methyl Ester Hydrochloride

https://huagongshe.com/reaction/1937403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-(3-Ethynyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic AcidHCID 22460834—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(3-Ethynyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic Acid Methyl Ester HydrochlorideHCID 8675809935%

Reaction Steps

To 4-(3-ethynyl-phenylamino)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid (0.108 g, 0.39 mmol) in dry methylene chloride (2 ml) was added a solution of oxalyl chloride (0.17 ml, 1.9 mmol) in dry methylene chloride (4 ml) followed by 1 drop of dry DMF. The suspension was stirred at ambient temperature for 1 hour, then concentrated in vacuo. To the resulting solid was added dry acetone (2 ml) and dry methanol (1 ml). The solution was stirred at ambient temperature for 15 hours, then concentrated in vacuo. The residue was diluted with ethyl acetate and water, and the solid filtered and dried in vacuo to afford the title compound as a tan powder (40 mg, 35%). TS-MS: 293 (MH+); anal. RP18-HPLC RT: min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395733B1
Source datasetuspto-grants-2002_05
ORD IDord-f310ae886dbb476d97de1426a77228fa
Source noteuspto-grants-2002_05