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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805759Generated: November 1, 2026

Isopropylamine → 7-Chloro-5-(isopropylamino)-3-methylpyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1805759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
Reactant5,7-dichloro-3-methylpyrido[4,3-d]pyrimidin-4(3H)-oneHCID 58092948—
Solvent1,4-DioxaneHCID 31275—
Product7-Chloro-5-(isopropylamino)-3-methylpyrido[4,3-d]pyrimidin-4(3H)-oneHCID 58092944—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5,7-dichloro-3-methylpyrido[4,3-d]pyrimidin-4(3H)-one (920.2 mg, 4.0 mmol) and isopropylamine (1.7 mL, 1.182 g, 20.0 mmol) in dioxane (10 mL) was heated at 80° C. for 26 hours and evaporated to result in a residue which was partitioned between saturated NH4Cl solution (200 mL) and EtOAc (100 mL). The aqueous phase was extracted with EtOAc (2×50 mL) and the combined organic phases were washed with brine (20 mL), dried over Na2SO4, and evaporated to afford crude title product. 1H NMR (DMSO-d6) 1.22 (d, J=6.4 Hz, 6H, 2CH3), 3.42 (s, 3H, NCH3), 4.19 (m, 1H), 6.59 (s, 1H), 8.45 (s, 1H), 8.90 (d, J=7.6 Hz, 1H, NH); ESI-MS m/z 253.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354526B2
Source datasetuspto-grants-2013_01
ORD IDord-ef28165f0d6f480cb52b78b99b33e307
Source noteuspto-grants-2013_01