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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085279Generated: November 1, 2026

Triphenylphosphine → HCID 20061223, compound

https://huagongshe.com/reaction/1085279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Methoxy-5-nitrophenolHCID 69471—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 20061251HCID 20061251—
ReactantHCID 20061272HCID 20061272—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20061223HCID 20061223—

Reaction Steps

Preparation of 1,3-dimethyl-6-{4-[3-(2-methoxy-5-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione hydrochloride (Compound 160) ##STR141## 0.9 g of 2-methoxy-5-nitrophenol, 1.0 g of 1,3-dimethyl-6-[4-(3-hydroxypropyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione (Compound 139) and 1.1 g of triphenylphosphine were suspended in 20 ml of anhydrous tetrahydrofuran, followed by the addition of 0.67 ml of diethyl azodicarboxylate. The thus-prepared mixture was treated in a similar manner to Example 84-(2), thereby obtaining 1.2 g of 1,3-dimethyl-6-{4-[3-(2-methoxy-5-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008267
Source datasetuspto-grants-1991_04
ORD IDord-cdb11c3ce3ed4b41acf5f470d5151a7e
Source noteuspto-grants-1991_04