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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082017Generated: October 29, 2026

2,4-Dichloroquinazoline → 4'-[[(2-Chloro-4-quinazolinyl)amino]methyl][1,1'-biphenyl]-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2082017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloroquinazolineHCID 252886—
ReactantSodium AcetateHCID 517045—
ReactantMethyl 2-[4-(aminomethyl)phenyl]benzoateHCID 1393434—
SolventTetrahydrofuranHCID 8028—
Product4'-[[(2-Chloro-4-quinazolinyl)amino]methyl][1,1'-biphenyl]-2-carboxylic acid methyl esterHCID 15233818—

Reaction Steps

Sodium acetate (0.65 g), 2,4-dichloroquinazoline (0.52 g) and 4'-aminomethyl[1,1'-biphenyl]-2-carboxylic acid methyl ester (0.73 g) were suspended in 25 mL of tetrahydrofuran. The reaction was stirred at room temperature for approximately 18 hours at which time the solvents were evaporated. The residue was loaded onto a silica gel column and the desired product was eluted with ethyl acetate/hexane (1:1). The yield was 0.75 g (71%) (m.p.=75°-90° C.): 1H NMR (DMSO-d6, 300 MHz) δ9.30 (t, J=6 Hz, 1H), 8.33 (d, J=8.1 Hz, 1H), 7.81 (m, 1H), 7.71 (m, 1H), 7.60 (m, 3H), 7.45 (m, 4H), 7.25 (d, J=8.1 Hz, 2H), 4.80 (d, J=5.8 Hz, 2H), 3.58 (s, 3H); positive FAB MS m/e 404(MH). Anal. calcd for C23H18ClN3O2 : C, 68.40; H, 4.49; N, 10.40. Found: C, 68.09; H, 4.57; N, 10.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187168
Source datasetuspto-grants-1993_02
ORD IDord-46ebdc165c5b4294874bc5d086cfff38
Source noteuspto-grants-1993_02