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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162966Generated: October 29, 2026

Diisopropylethylamine → 7-(2-Butyn-1-yl)-8-[(3R)-3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-piperidinyl]-3,7-dihydro-3-methyl-1-[(4-methyl-2-quinazolinyl)methyl]-1H-purine-2,6-dione

https://huagongshe.com/reaction/1162966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant8-Bromo-7-but-2-ynyl-3-methyl-1-[(4-methylquinazolin-2-yl)methyl]purine-2,6-dioneHCID 24750049—
Reactant3-(Phthalimido)piperidine d-tartrateHCID 66704149—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product7-(2-Butyn-1-yl)-8-[(3R)-3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-piperidinyl]-3,7-dihydro-3-methyl-1-[(4-methyl-2-quinazolinyl)methyl]-1H-purine-2,6-dioneHCID 59522528—

Reaction Conditions

Temperature140 °C

Reaction Steps

10.00 kg (22.06 mol) of 1-[(4-methylquinazolin-2-yl)methyl]-3-methyl-7-(2-butin-1-yl)-8-bromoxanthine, 12.59 kg (33.09 mol) of 3-(phthalimido)piperidine D-tartrate and 17.5 litres of N-methyl-2-pyrrolidone are initially charged in the reactor. The reactor contents are heated to 140° C. After the temperature has been attained, 11.41 kg (88.24 mol) of diisopropylethylamine are metered in within 20 minutes. The feed vessel is flushed with 2.5 litres of N-methyl-2-pyrrolidone and the reaction mixture is subsequently stirred at 140° C. for 2 hours. After the reaction has ended, the reaction mixture is cooled to 60° C. and diluted with 80 litres of methanol. The resulting suspension is stirred at 50° C. for 30 minutes, then cooled to 23° C. and stirred for a further 30 minutes. Subsequently, the product is centrifuged off and washed 3 times with 20 litres each time of methanol. Drying is effected at 45° C. in a drying cabinet under inertization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820815B2
Source datasetuspto-grants-2010_10
ORD IDord-53fba3e034804466ba2074f06c2d63de
Source noteuspto-grants-2010_10