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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409681Generated: October 29, 2026

Triethylamine → HCID 69252826, compound

https://huagongshe.com/reaction/409681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-EthylpiperazineHCID 79196—
ReactantPropylphosphoric anhydrideHCID 16167369—
ReactantHCID 69162548HCID 69162548—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 69252826HCID 69252826—

Reaction Steps

Propylphosphonic anhydride (50% in DMF, 2.72 mL, 4.7 mmol, 2 equiv) is added to a solution of 4-(6-methylamino-pyrimidin-4-ylamino)-benzoic acid (0.570 g, 2.33 mmol), N-ethyl-piperazine (0.33 mL, 2.57 mmol, 1.1 equiv), DMAP (7 mg), and Et3N (3.3 mL, 23.3 mmol, 10 equiv) in DMF (25 mL), at RT and under an argon atmosphere. The reaction mixture is stirred at RT for 1 h, diluted with EtOAc and washed with H2O. The aqueous layer is extracted with EtOAc. The combined organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. The residue is purified by silica gel column chromatography (DCM→DCM/2 N NH3 in MeOH, 86:14) to provide the title compound as a yellow foam: ES-MS: 341.2 [MH]+; tR=1.00 min (system 1); Rf=0.33 (CH2Cl2/2 N NH3 in MeOH, 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759517B2
Source datasetuspto-grants-2014_06
ORD IDord-b639a771c2b041799caf3f8c9be00235
Source noteuspto-grants-2014_06