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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53170Generated: October 29, 2026

6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one → 6-Acetyl-2-benzyloxyoxazolo[4,5-b]pyridine

https://huagongshe.com/reaction/53170

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-oneHCID 15926016—
Reactant2-(Benzyloxy)-6-bromo[1,3]oxazolo[4,5-b]pyridineHCID 19079302—
Product6-Acetyl-2-benzyloxyoxazolo[4,5-b]pyridineHCID 19079308—

Reaction Steps

The method of operation is the same as that used for the synthesis of the compound of Example 1 (coupling with 1-ethoxy-1-(trimethylstannyl)ethylene), 2-benzyloxy-6-bromooxazolo[4,5-b]pyridine from Preparation 4 being used instead of the 6-bromo-3-methyloxazolo[4,5-b]pyridin-2(3H)-one from Preparation 2. The yield obtained is 78%. ##STR49##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618819
Source datasetuspto-grants-1997_04
ORD IDord-54b4091bbb124d768a7411fc5e06240b
Source noteuspto-grants-1997_04