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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181685Generated: October 31, 2026

Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) → 7-Isobutyl-5-(2-morpholin-4-ylethyl)-2-(1-naphthylmethyl)-3-pyridin-4-yl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione

https://huagongshe.com/reaction/1181685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant7-isobutyl-2-(1-naphthylmethyl)-3-pyridin-4-yl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dioneHCID 69427445—
SolventDimethylformamideHCID 6228—
Product7-Isobutyl-5-(2-morpholin-4-ylethyl)-2-(1-naphthylmethyl)-3-pyridin-4-yl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dioneHCID 5898091491.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(2-chloroethyl)morpholine hydrochloride (0.0435 g) followed by DBU (0.094 g) were added to a solution of 7-isobutyl-2-(1-naphthylmethyl)-3-pyridin-4-yl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione (0.0668 g) in dimethylformamide (1 ml). The mixture was heated at 80° C. for 18 hours then cooled to room temperature. The crude reaction was purified on preparative HPLC to give the title compound (0.077 g). Mass: 538.90 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285558B2
Source datasetuspto-grants-2007_10
ORD IDord-f253712b955c4370ae2ee2831182f521
Source noteuspto-grants-2007_10