Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420940Generated: October 31, 2026

Water → Methyl 5-chloropyrimido(4,5-c)quinoline-8-carboxylate

https://huagongshe.com/reaction/2420940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylateHCID 50942144—
SolventTolueneHCID 1140—
ProductMethyl 5-chloropyrimido(4,5-c)quinoline-8-carboxylateHCID 5094224271.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a vial, methyl 5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylate (1.0 eq, 151 mg, 0.59 mmol) was mixed in toluene (1 ml) with DIEA (1.5 eq, 155 ul, 0.89 mmol) and POCl3 (5 eq, 270 ul, 3.0 mmol). The mixture was stirred at 120° C. for 1 hour and cooled down to room temperature. After adding ice and water the compound was extracted with CH2Cl2 (4×). The solution was filtered over Na2SO4 and filtered through a pad of celite. After evaporation of the volatiles, the material was triturated in a mixture of ethyl acetate and hexanes, filtered and dried to afford methyl 5-chloropyrimido[4,5-c]quinoline-8-carboxylate as a light brown fluffy solid (115 mg, 71% yield). LCMS (ES): 95% pure, m/z 274 [M+1]+. 1H NMR (DMSO-d6, 400 MHz) δ 3.96 (s, 3H), 8.37 (dd, J=1.6, J=8.4, 1H), 8.60 (d, J=1.6, 1H), 9.15 (d, J=8.8, 1H), 9.74 (s, 1H), 10.61 (s, 1H) ppm

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956064B2
Source datasetuspto-grants-2011_06
ORD IDord-269c0073be0f4993951ecb0cca4a0a98
Source noteuspto-grants-2011_06