Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491342Generated: October 31, 2026

Oxalyl chloride → 5-(1,1-Dimethylethyl) 1-ethyl 4,6-dihydro-3-[[2-(2-naphthalenyl)-1-oxopropyl]amino]pyrrolo[3,4-c]pyrazole-1,5-dicarboxylate

https://huagongshe.com/reaction/491342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-tert-Butyl 1-ethyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-1,5-dicarboxylateHCID 6919045—
Reactant13350-60-2HCID 13147846—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexane ethylacetateHCID 21867204—
Product5-(1,1-Dimethylethyl) 1-ethyl 4,6-dihydro-3-[[2-(2-naphthalenyl)-1-oxopropyl]amino]pyrrolo[3,4-c]pyrazole-1,5-dicarboxylateHCID 6844152493%

Reaction Steps

To a solution of 2-naphthalen-2-yl-propionic acid (1.48 g. 7.4 mmol) in DCM (40 ml) and DMF cat., (COCl)2 (0.83 ml, 9.65 mmol) in DCM (10 ml) was added dropwise. The mixture was stirred at r.t. for 30 min. The reaction mixture was concentrated under vacuum, reconstituted twice with toluene and concentrated. A solution of the obtained acyl-chloride in THF (40 ml) was added slowly to a mixture of 3-amino-4,6-dihydro-pyrrolo[3,4-c]pyrazole-1,5-dicarboxylic acid 5-tert-butyl ester 1-ethyl ester (2.0 g, 6.75 mmol) and DIEA (5.8 ml, 33.3 mmol) in THF (40 ml) at 0-5° C. The reaction was allowed to reach r.t. and stirred overnight. The mixture was filtered and the solution evaporated to dryness under vacuum. The resulting residue was dissolved in DCM and the obtained solution washed with brine, dried over sodium sulfate, filtered and evaporated to dryness. The crude product was purified by flash-chromatography (eluent:ethyl acetate/cyclohexane 3/7 then 4/6) to give 3.0 g (93% yield) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531531B2
Source datasetuspto-grants-2009_05
ORD IDord-96b2a106b0d04829881704f13a880246
Source noteuspto-grants-2009_05