Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626550Generated: October 27, 2026

1,2-Dichloroethane → (S)-1-(4-(6-(cyclopropanecarbonyl)-4-(3-methylmorpholino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)-3-cyclopropylurea

https://huagongshe.com/reaction/1626550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantCyclopropanecarboxylic acidHCID 15655—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-1-cyclopropyl-3-(4-(4-(3-methylmorpholino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)ureaHCID 46894114—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(S)-1-(4-(6-(cyclopropanecarbonyl)-4-(3-methylmorpholino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)-3-cyclopropylureaHCID 4691228237%

Reaction Steps

To a stirred solution of (S)-1-cyclopropyl-3-(4-(4-(3-methylmorpholino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)urea (example 3) (150 mg, 0.38 mmol) in 2-methyl THF (2 mL) and DMSO (1 mL) was added DIPEA (159 uL, 0.92 mmol), cyclopropane carboxylic acid (578 uL, 0.73 mmol) and EDC (139 mg, 0.73 mmol), followed by HOBt (98 mg, 0.73 mmol). The reaction mixture was stirred at room temperature for 4 h then diluted with water and ethyl acetate. The organic layer was concentrated and purified by prep HPLC (low pH) to give a pale yellow solid (65 mg, 0.14 mmol, 37% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785457B2
Source datasetuspto-grants-2014_07
ORD IDord-fe4e7332113a4d8db0b0e7262a28c594
Source noteuspto-grants-2014_07