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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892119Generated: October 30, 2026

Triethylamine → (S)-N-(3-bromo-4-fluorophenyl)-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperazine-1-carboxamide

https://huagongshe.com/reaction/1892119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant3-Bromo-4-fluoroanilineHCID 2779286—
Reactant(S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 68958720—
SolventDichloromethaneHCID 6344—
Product(S)-N-(3-bromo-4-fluorophenyl)-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperazine-1-carboxamideHCID 4454307914.5%

Reaction Steps

To a solution of triphosgene (0.30 g, 1 mmol) in CH2Cl2 (70 ml) at −5° C. were added 3-bromo-4-fluoroaniline (0.19 g, 1 mmol) in CH2Cl2 (20 ml) and triethylamine (0.60 ml, 4.3 mmol). The reaction was stirred at room temperature for 20 min, then (S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine from step B (0.23 g, 1 mmol) in CH2Cl2 (30 ml) was added. The mixture was stirred for 1.5 hours, then concentrated under vacuum. The residue was purified by prep HPLC to afford (S)—N-(3-bromo-4-fluorophenyl)-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperazine-1-carboxamide (65 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507672B2
Source datasetuspto-grants-2013_08
ORD IDord-5d390de8ccc546e8a274e685328a3676
Source noteuspto-grants-2013_08