HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine → {2-Methyl-4-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-phenylsulfanyl}-acetic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine | HCID 21935751 | — |
| Reactant | (4-Hydroxy-2-methyl-phenylsulfanyl)-acetic acid tert-butyl ester | HCID 67072245 | — |
| Product | {2-Methyl-4-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-phenylsulfanyl}-acetic acid tert-butyl ester | HCID 67072399 | — |
Reaction Steps
In analogy to the procedure described in example 20A], (4-hydroxy-2-methyl-phenylsulfanyl)-acetic acid tert-butyl ester (example 20C]), was reacted with 3-chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine (example 1N]) to give {2-methyl-4-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-phenylsulfanyl}-acetic acid tert-butyl ester, which was subsequently saponified in analogy to the procedure described in example 20B] to yield the title compound as white solid of mp. 168–169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115611B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-76d191a87f2b4ba6960fade82f3019c2 |
| Source note | uspto-grants-2006_10 |