HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Tributylstannyl)methanol → N-(4-(2-(Hydroxymethyl)-6-(4-(trifluoromethyl)phenyl)pyrimidin-4-yloxy)-benzo[d]thiazol-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Tributylstannyl)methanol | HCID 4193593 | — |
| Reactant | N-{4-[2-chloro-6-(4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzo[d]thiazol-2-yl}-acetamide | HCID 58612070 | — |
| Product | N-(4-(2-(Hydroxymethyl)-6-(4-(trifluoromethyl)phenyl)pyrimidin-4-yloxy)-benzo[d]thiazol-2-yl)acetamide | HCID 11518253 | — |
Reaction Steps
The reaction of N-{4-[2-chloro-6-(4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-benzo[d]thiazol-2-yl}-acetamide (233 mg, 0.5 mmol, Example 7(d)) and tributylstannyl-methanol (322 mg, 1.0 mmol, prepared according to the procedure described in Synthetic Communication, 1994, 24, 1117-1120) under the conditions of Example 7(e) gave the title compound as a white amorphous solid. MS (ESI, pos. ion) m/z: 461 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335672B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-8485dd9fb30f404281de78fa8e58ac20 |
| Source note | uspto-grants-2008_02 |