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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085281Generated: October 30, 2026

Triphenylphosphine → HCID 20061254, compound

https://huagongshe.com/reaction/1085281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 20061251HCID 20061251—
ReactantHCID 20061337HCID 20061337—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20061254HCID 2006125479.4%

Reaction Steps

0.7 g of 2-benzylamino-4-nitrophenol, 0.8 g of 1,3-dimethyl-6-[4-(3-hydroxypropyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione (Compound 139) and 0.9 g of triphenylphosphine were suspended in 20 ml of anhydrous tetrahydrofuran, followed by the addition of 0.65 g of diethyl azodicarboxylate. The thus-prepared mixture was treated in a similar manner to Example 84-(2), thereby obtaining 0.93 g of 1,3-dimethyl-6-{4-[3-(2-benzylamino-4-nitrophenyloxy)propyl]piperazin-1yl}-2,4(1H,3H)-pyrimidinedione as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008267
Source datasetuspto-grants-1991_04
ORD IDord-dcb30a4711e2425fa2f0c9b165eb92f2
Source noteuspto-grants-1991_04