Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892139Generated: October 27, 2026

Triethylamine → (S)-N-(3-bromophenyl)-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N'-(methylsulfonyl)piperazine-1-carboximidamide

https://huagongshe.com/reaction/1892139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantphenyl N-3-bromophenyl-N'-(methylsulfonyl)carbamimidateHCID 68725987—
Reactant(S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 68958720—
SolventAcetonitrileHCID 6342—
Product(S)-N-(3-bromophenyl)-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N'-(methylsulfonyl)piperazine-1-carboximidamideHCID 68957478—

Reaction Steps

The carbamimidate from step B (100 mg, 0.27 mmol), (S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine, from Example 1, step B (63 mg, 0.27 mmol), and triethylamine (77 μl, 0.27 mmol) were combined in MeCN (1.5 ml) and heated to reflux for 2 hours. The mixture was concentrated and purified by preparative HPLC to afford (S)—N-(3-bromophenyl)-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N′-(methylsulfonyl)piperazine-1-carboximidamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507672B2
Source datasetuspto-grants-2013_08
ORD IDord-664ab8a1e0fa4135be5a8ddf6830ef78
Source noteuspto-grants-2013_08