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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892125Generated: October 27, 2026

Triethylamine → HCID 178430829, compound

https://huagongshe.com/reaction/1892125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 68958720—
ReactantHCID 178512251HCID 178512251—
ReactantHCID 178512407HCID 178512407—
SolventIsopropanolHCID 3776—
ProductHCID 178430829HCID 178430829—

Reaction Conditions

Temperature140 °C

Reaction Steps

Phenyl N′-cyano-N-(3-(trifluoromethyl)phenyl)carbamimidate, prepared analogously to N-3-bromophenyl-N′-cyanocarbamimidate from Example 5, step A (36 mg, 0.12 mmol), (S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine, from Example 1, step B, (35 mg, 0.15 mmol), and triethylamine (0.05 ml, 0.36 mmol) were combined in isopropanol in a microwave vessel. The reaction was heated at 140° C. for 30 min. under microwave conditions. The solvent was evaporated, and the residue was washed with CH2Cl2 (3×10 ml). The crude product was purified by Prep-HPLC to afford (S)—N′-cyano-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N-(3-(trifluoromethyl)phenyl)-piperazine-1-carboximidamide as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507672B2
Source datasetuspto-grants-2013_08
ORD IDord-c797dc14195d49fb8f07366ff2eca363
Source noteuspto-grants-2013_08