HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-bromo-3-benzyloxazolo[4,5-b]pyridin-2(3H)-one → HCID 15379437, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-bromo-3-benzyloxazolo[4,5-b]pyridin-2(3H)-one | HCID 13614468 | — |
| Reactant | 6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one | HCID 15926016 | — |
| Product | HCID 15379437 | HCID 15379437 | — |
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), 6-bromo-3-benzyloxazolo[4,5-b]pyridin-2(3H)-one from Preparation 13 being used instead of 6-bromo-3-methyloxazolo[4,5-b]pyridin-2(3H)-one. The yield obtained is 75%. ##STR47##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05767128 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-4e0c3ae897964fd298ebf6bbcd22aa39 |
| Source note | uspto-grants-1998_06 |