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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66384Generated: October 30, 2026

Dimethylformamide → 2-[3-(2-Dimethylaminoethoxy)phenyl]oxazolo[4,5-b]pyridine

https://huagongshe.com/reaction/66384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium MethoxideHCID 10942334—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
ReactantHCID 16127331HCID 16127331—
SolventDiethyl EtherHCID 3283—
Product2-[3-(2-Dimethylaminoethoxy)phenyl]oxazolo[4,5-b]pyridineHCID 22754792—

Reaction Steps

To a solution of 1.1 g. (0.005 mole) of 2-(3-hydroxyphenyl)oxazolo[4,5-b]pyridine in 15 ml. dried dimethylformamide is added 0.6 g. (0.011 mole) of sodium methoxide in portions over about 10 min. To the reddish-orange solution cooled in an ice-bath is added 0.72 g. (0.005 mole) of N,N-dimethyl-2-chloroethylamine hydrochloride in portions over 15 minutes. The resultant mixture is then stirred 10 minutes, set in an oil-bath at 75° C., and kept at 75-90° C. (bath) for 20 hours. After cooling to room temperature, 15 ml. of dried ether is added with stirring, and the resultant mixture is filtered. The filtrate is then stripped of solvent, and the residue distributed between methylene chloride and water. The organic layer is dried over sodium sulfate, filtered, and concentrated in vacuo to yield 2-[3-(2-dimethylaminoethoxy)phenyl]oxazolo[4,5-b]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04131677
Source datasetuspto-grants-1978_12
ORD IDord-c271a9dab13444438170bbd2b80084db
Source noteuspto-grants-1978_12