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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496868Generated: October 30, 2026

Triphenylphosphine → 2-((7-Bromoquinolin-5-yloxy)methyl)nicotinamide

https://huagongshe.com/reaction/1496868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant2-(Hydroxymethyl)pyridine-3-carboxamideHCID 13929518—
Reactant7-Bromoquinolin-5-olHCID 136216619—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-((7-Bromoquinolin-5-yloxy)methyl)nicotinamideHCID 7123777545%

Reaction Steps

100 mg 7-Bromo-quinolin-5-ol, 77.5 mg of 2-(hydroxymethyl)nicotinamide 3.7, 233.5 mg of triphenylphosphine and 205 mg of Di-tertbutyl-azodicarboxylate (DBAD) were dissolved in 2.5 mL of DCM and 7.5 mL of THF under Argon at room temperature. After 14 h the precipitate was collected and dried. The mother liquor was concentrated and the formed precipitate again collected to yield 72 mg Example 22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199937B2
Source datasetuspto-grants-2015_12
ORD IDord-d500ee0a7eb943658494ddda191f802a
Source noteuspto-grants-2015_12