HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-(5,9-Dioxaspiro[3.5]non-7-yloxy)pyridin-2-yl)methanol → HCID 66776211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-(5,9-Dioxaspiro[3.5]non-7-yloxy)pyridin-2-yl)methanol | HCID 59792459 | — |
| Reactant | HCID 66776433 | HCID 66776433 | — |
| Product | HCID 66776211 | HCID 66776211 | — |
Reaction Steps
The same procedure as in the steps (9h) to (9j) of Example 9 was repeated using the (4-(5,9-dioxaspiro[3.5]non-7-yloxy)pyridin-2-yl)methanol obtained in the step (83b) above to obtain the title compound (100 mg, the total yield of 3 steps: 50%) as a white solid. Note that, in the same process as in the step (9h), 2-mercaptobenzimidazole was added to the reaction mixture and stirred at room temperature for 25 hours, and thereafter, 3 equivalents of potassium hydroxide relative to the alcohol was added thereto. The mixture was allowed to react at room temperature for 6 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124780B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-1e992ff1e34f496fbd73ad93a55e7bc9 |
| Source note | uspto-grants-2012_02 |