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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50807Generated: October 25, 2026

2-(Aminomethyl)aniline → 4-N-[(2-aminophenyl)methyl]pyrido[4,3-d]pyrimidine-4,7-diamine

https://huagongshe.com/reaction/50807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Aminomethyl)anilineHCID 178096—
Reactant7-Amino-4-methylthiopyrido[4,3-d]pyrimidineHCID 10442562—
SolventIsopropanolHCID 3776—
Product4-N-[(2-aminophenyl)methyl]pyrido[4,3-d]pyrimidine-4,7-diamineHCID 532809047.1%

Reaction Steps

A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (136 mg, 0.71 mmol) (described in a previous experimental) and 2-aminobenzylamine (1.70 g, 13.8 mmol) in isopropanol (5 mL) is stirred at reflux for 1 h, and the resulting product is chromatographed on silica gel (7-20% EtOH/EtOAc) and alumina (6-10i EtOH/CHCl3) to give 7-amino-4-(2-aminobenzylamino)pyrido[4,3-d]pyrimidine (89 mg, 47%) as a white solid. 1H NMR (DMSO) δ 9.08 (1H, s), 8.68 (1H, t, J=5.8 Hz), 8.26 (1H, s), 7.05 (1H, d, J=7.4 Hz), 6.96 (1H, t, J=7.6 Hz), 6.63 (1H, d, J=7.9 Hz), 6.51 (1H, t, J=7.4 Hz), 6.46 (2H, brs), 6.35 (1H, s), 5.20 (2 H, brs), 4.56 (2H, d, J=5.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713484B2
Source datasetuspto-grants-2004_03
ORD IDord-00b2002f949b45f49006c6d5f022bf42
Source noteuspto-grants-2004_03