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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241574Generated: October 30, 2026

Triphenylphosphine → HCID 21936093, compound

https://huagongshe.com/reaction/1241574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-PyrrolidineethanolHCID 76288—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 135594114HCID 135594114—
SolventDichloromethaneHCID 6344—
ProductHCID 21936093HCID 2193609312.9%

Reaction Steps

Diethyl azodicarboxylate (0.182 ml) was added dropwise to a stirred mixture of 4-(6-chloro-2,3-methylenedioxyanilino)-7-hydroxy-6-methoxyquinazoline (0.2 g), N-(2-hydroxyethyl)pyrrolidine (0.086 g), triphenylphosphine (0.303 g) and methylene chloride (3 ml) and the reaction mixture was stirred at ambient temperature for 15 minutes. The reaction mixture was evaporated and the residue was purified by column chromatography on silica using a 45:4:1 mixture of methylene chloride, methanol and a saturated methanolic ammonia solution as eluent. There was thus obtained the title compound (0.033 g) as a white solid; NMR Spectrum: (DMSOd6 and CF3CO2D) 1.9 (m, 2H), 2.1 (m, 2H), 3.2 (m, 2H), 3.7 (m, 2H), 3.8 (m, 2H), 4.05 (s, 3H), 4.6 (m, 2H),6.2 (s, 2H), 7.1 (d, 1H), 7.5 (s, 1H), 8.2 (s, 1H), 8.95 (s, 1H); Mass Spectrum: M−H− 441 and 443.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115615B2
Source datasetuspto-grants-2006_10
ORD IDord-5d84eb2fe9b04c2dbbcea67c2db48ea4
Source noteuspto-grants-2006_10