HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromoindoline → 5-Bromo-1-[2-(pyridin-2-ylmethyloxy)pyridin-5-ylcarbamoyl]-indoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromoindoline | HCID 3411566 | — |
| Reactant | Phenyl N-[2-(pyridin-2-ylmethyloxy)pyridin-5-yl]carbamate | HCID 11141770 | — |
| Product | 5-Bromo-1-[2-(pyridin-2-ylmethyloxy)pyridin-5-ylcarbamoyl]-indoline | HCID 18357723 | — |
Reaction Steps
Phenyl N-[2-(pyridin-2-ylmethyloxy)pyridin-5-yl]carbamate (D3) and 5-bromoindoline were converted into the title compound using a method similar to that of Example 1, m.p. 138-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313145B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-b742c408adf44ec58e4fd583a05b8d71 |
| Source note | uspto-grants-2001_11 |