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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371117Generated: November 2, 2026

Piperazine → HCID 178433086, compound

https://huagongshe.com/reaction/1371117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178432852HCID 178432852—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178433086HCID 17843308629.1%

Reaction Steps

This compound was prepared according to the method described in Example 26 by employing 4-chloro-2-methyl-6-phenylpyrrolo[3,2-d]pyrimidine (Example 1(e)) (0.10 g, 0.41 mmol), piperazine (Aldrich Chemical Company) (0.382 g, 4.43 mmol) and K2CO3 (0.34 g, 2.50 mmol) in H2O (2.5 mL) to give crude pink solids. These solids were taken up in hot EtOAc, cooled to room temperature, and the impurities were removed by filtration. The filtrate was concentrated to give 0.035 g (29%) of the title compound as an off-white solid. Mp: 236° C. 1H NMR (DMSO-d6; 500 MHz): δ 2.42 (s, 3), 2.85 (t, 4, J=5.2), 3.62 (t, 4, J=5.2), 6.77 (s, 1), 7.36 (m, 1), 7.45 (t, 2, J=7.8), 7.95 (d, 2, J=7.6), 10.96 (s, 1); MS m/z: 294 (M+1). Anal. Calcd for C17H19N5O.0.5H2O: C, 67.53; H, 6.67; N, 23.16. Found: C, 67.35; H, 6.59; N, 23.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583154B1
Source datasetuspto-grants-2003_06
ORD IDord-14b977dba4194706b8e9bfc7c38cd904
Source noteuspto-grants-2003_06