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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655335Generated: October 29, 2026

2-(Dimethylamino)ethanol → HCID 58486118, compound

https://huagongshe.com/reaction/655335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantHCID 58486100HCID 58486100—
SolventDimethylformamideHCID 6228—
ProductHCID 58486118HCID 58486118—

Reaction Steps

100 mg (0.3 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 30 μl (0.3 mmol) of 2-dimethylaminoethanol are added successively to a suspension of 67 mg (0.2 mmol) of 3-[3-(5-hydroxypyrimidin-2-yl)benzyl]-5-methyl-3H-oxazolo[4,5-b]pyridin-2-one in 3 ml of DMF. 69 mg (0.30 mmol) of di-tert-butyl azodicarboxylate are subsequently added. The reaction mixture is shaken at room temperature for 18 hours. A further 100 mg (0.3 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 69 mg (0.30 mmol) of di-tert-butyl azodicarboxylate are added, and the mixture is shaken at room temperature for 18 h. A further 100 mg (0.3 mmol) of polymer-bound triphenylphosphine (3 mmol/g), 69 mg (0.30 mmol) of di-tert-butyl azodicarboxylate and 30 μl (0.3 mmol) of 2-dimethylaminoethanol are subsequently added, and the mixture is shaken at room temperature for 18 h. The reaction mixture is filtered, the filtrate is evaporated in vacuo, and the residue is purified by column chromatography on silica gel, giving “A109”. The crude product is purified by preparative HPLC; ESI: 406; HPLC: Rt=2.31 min (method B);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071593B2
Source datasetuspto-grants-2011_12
ORD IDord-47b42fae22dd48729600e5d1d5b4f255
Source noteuspto-grants-2011_12