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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255899Generated: October 30, 2026

Triphenylphosphine → HCID 58174058, compound

https://huagongshe.com/reaction/1255899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantp-(Benzyloxy)phenethyl alcoholHCID 3017260—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 58174068HCID 58174068—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58174058HCID 5817405820%

Reaction Steps

4-[2-(Pteridin-4-ylamino)-ethyl]-phenol (300 mg, 10.1 mmol), triphenylphosphine (790 mg, 3.0 mmol) and 2-(4-benzyloxyphenyl)ethanol (700 mg, 3.0 mmol) were combined in 10 mL anh. dioxane, treated with diisopropylazodicarboxylate (590 μL, 610 mg, 3.0 mmol) and stirred for 18 h. The volatiles were removed in vacuo and the residue was chromatographed on SiO2 with EtOAc (10% to 40%) in CH2Cl2 to obtain (2-{4-[2-(4-benzyloxyphenyl)-ethoxy]-phenyl}-ethyl)-pteridin-4-ylamine (105 mg; 20%) as a white solid: mp 120-122° C.; ESIMS m/z 478 ([M+H]+); 1H NMR (300 MHz, CDCl3) δ 9.23 (s, 1H), 8.96 (s, 1H), 8.80 (s, 1H), 6.8-7.5 (m, 13H), 4.1 (m, 2H), 3.90 (m, 2H), 3.01 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461164B2
Source datasetuspto-grants-2013_06
ORD IDord-a495e067096c4d43bf51bcfb96f5ca5f
Source noteuspto-grants-2013_06