HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one → 6-Acetyl-2-benzyloxyoxazolo[4,5-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one | HCID 15926016 | — |
| Reactant | 2-(Benzyloxy)-6-bromo[1,3]oxazolo[4,5-b]pyridine | HCID 19079302 | — |
| Product | 6-Acetyl-2-benzyloxyoxazolo[4,5-b]pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05618819 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-54b4091bbb124d768a7411fc5e06240b |
| Source note | uspto-grants-1997_04 |