Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567746Generated: October 26, 2026

1-Methylpiperazine → HCID 9928658, compound

https://huagongshe.com/reaction/567746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant4-(3-chloroanilino)-6-formyl-7H-pyrrolo[2,3-d]pyrimidineHCID 11097699—
CatalystNickelHCID 935—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 9928658HCID 9928658—

Reaction Steps

136.4 mg (0.50 mmol) of 4-(3-chloroanilino)-6-formyl-7H-pyrrolo[2,3-d] pyrimidine and 67 μl of N-methylpiperazine in 5 ml of methanol, 15 ml of DMPU and 63 μl of acetic acid are hydrogenated at 50° C. in the presence of 30 mg of Raney nickel. The catalyst is filtered off, the filtrate is evaporated and the residue is dissolved in ethyl acetate and satd NaHCO3 solution. The aqueous phase separated off is extracted twice with ethyl acetate; the organic phases are washed with satd NaHCO3 solution, 4 times with water and brine, dried over Na2SO4 and evaporated. Column chromatography (SiO2, CH2Cl2/methanol=7:2) and stirring in diethyl ether yields 4-(3-chloroanilino)-6-[(4-methylpiperazin-1-yl)methyl]-7H-pyrrolo[2,3-d]pyrimidine; HPLC: tRet(Grad20)=7.4; TLC-Rf=0.16 (CH2Cl2/methanol=7:3); FAB-MS: (M+H)+=357.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180636B2
Source datasetuspto-grants-2001_01
ORD IDord-ad0cf83e282e426fa1e6a6eea85b34a6
Source noteuspto-grants-2001_01