HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(Trifluoromethyl)indoline → 1-[2-(Pyridin-2-ylmethyloxy)pyridin-5ylcarbamoyl]-6-trifluoromethyl-indoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(Trifluoromethyl)indoline | HCID 10176437 | — |
| Reactant | Phenyl N-[2-(pyridin-2-ylmethyloxy)pyridin-5-yl]carbamate | HCID 11141770 | — |
| Product | 1-[2-(Pyridin-2-ylmethyloxy)pyridin-5ylcarbamoyl]-6-trifluoromethyl-indoline | HCID 18357724 | — |
Reaction Steps
Phenyl N-[2-(pyridin-2-ylmethyloxy)pyridin-5-yl]carbamate (D3) and 6-trifluoromethylindoline (WO 96/23783) were converted into the title compound using a method similar to that of Example 1, m.p. 178-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313145B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-2214641fc5e04914b17eb86118a03c30 |
| Source note | uspto-grants-2001_11 |