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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567754Generated: October 30, 2026

Acetic Acid → HCID 21262613, compound

https://huagongshe.com/reaction/567754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-MethoxybenzylamineHCID 75452—
Reactant4-(3-chloroanilino)-6-formyl-7H-pyrrolo[2,3-d]pyrimidineHCID 11097699—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 21262613HCID 21262613—

Reaction Steps

273 mg (1.00 mmol) of 4-(3-chloroanilino)-6-formyl-7H-pyrrolo[2,3-d]pyrimidine (stage 1.6) and 156 ml (1.2 mmol) of 4-methoxybenzylamine in 10 ml of methanol, DMPU and 126 μl (2.2 mmol) of acetic acid are stirred at RT for 1 h. 0.1 g of Raney nickel is then added and the mixture is hydrogenated at RT and finally at 50° C. The catalyst is filtered off, the filtrate is evaporated and the residue is dissolved in ethyl acetate and satd Na2CO3 solution. The aqueous phase separated off is extracted twice with ethyl acetate; the organic phases are washed with satd NaHCO3 solution, and twice with water and brine, dried (MgSO4) and evaporated. Stirring the residue in diethyl ether yields 4-(3-chloroanilino)-6-[(4-methoxybenzylamino)-methyl]-7H-pyrrolo[2,3-d]pyrimidine; HPLC: tRet(Grad20)=9.5; TLC-Rf=0.17 (CH2Cl2/methanol=10:1); FAB-MS: (M+H)+=394.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180636B2
Source datasetuspto-grants-2001_01
ORD IDord-6a1fd1ff8b964d89a98a0bc8f300c2f6
Source noteuspto-grants-2001_01