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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256147Generated: October 29, 2026

3-(aminomethyl)-N,N-dimethylaniline → Pyrido[4,3-d]pyrimidine-4,7-diamine,n4-[[3-(dimethylamino)phenyl]methyl]-

https://huagongshe.com/reaction/2256147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(aminomethyl)-N,N-dimethylanilineHCID 2760938—
Reactant7-Amino-4-methylthiopyrido[4,3-d]pyrimidineHCID 10442562—
SolventIsopropanolHCID 3776—
ProductPyrido[4,3-d]pyrimidine-4,7-diamine,n4-[[3-(dimethylamino)phenyl]methyl]-HCID 532809440%

Reaction Steps

A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (236 mg, 1.23 mmol) (described in a previous experimental) and 3-dimethylamino-benzylamine (1.36 g, 9.07 mmol) in isopropanol (5 mL) is stirred under N2 at reflux for 1 h, and the resulting product is chromatographed on silica gel (10-15% EtOH/EtOAc), then on alumina (1% EtOH/CHCl3) to give 7-amino-4-(3-dimethylaminobenzylamino)pyrido[4,3-d]pyrimidine (145 mg, 40%) as a white solid. 1H NMR (DMSO) δ 9.11 (1H, s), 8.79 (1H, t, J=5.9 Hz), 8.26 (1H, s), 7.11 (1H, dd, J=8.0, 7.7 Hz), 6.73 (1H, brs), 6.63 (1H, d, J=7.6 Hz), 6.60 (1H, dd, J=8.1, 2.2 Hz), 6.44 (2H, brs), 6.35 (1H, s), 4.67 (2H, d, J=5.8 Hz), 2.86 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654307
Source datasetuspto-grants-1997_08
ORD IDord-478981fc33f145d984724b75036ee301
Source noteuspto-grants-1997_08