Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169318Generated: November 3, 2026

Triphenylphosphine → 9-benzyloxy-2-cyclopropyl-6-(1-phenyl-cyclopentylmethyl)-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione

https://huagongshe.com/reaction/2169318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 178519962HCID 178519962—
SolventDichloromethaneHCID 6344—
Product9-benzyloxy-2-cyclopropyl-6-(1-phenyl-cyclopentylmethyl)-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dioneHCID 8672595762.3%

Reaction Steps

To a stirred solution of 5-benzyloxy-6-hydroxy-2-(1-phenyl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid cyclopropyl-(2-hydroxyethyl)-amide (285) (300 mg, 0.62 mmol) in dichloromethane (30 mL) were added triphenyl phosphine (242 mg, 0.92 mmol) and diisopropyl azodicarboxylate (0.2 mL, 1.23 mmol) at room temperature. Stirring was continued for 10 min at room temperature. The reaction mixture was concentrated under reduced pressure to get a crude product, which was purified by Combi-Flash column (triphenyl phosphine oxide was eluted in ethyl acetate and the product was eluted at 2% methanol in dichloromethane). It was again purified by preparative TLC plate to remove traces of triphenyl phosphine oxide (mobile phase: ethyl acetate) and 9-benzyloxy-2-cyclopropyl-6-(1-phenyl-cyclopentylmethyl)-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione (286) (180 mg, 62.3%) was obtained as a white sticky solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-2404fa5399b3419892948e761e014c6d
Source noteuspto-grants-2015_06