HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 58968667, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Dimethyl Ether | HCID 8254 | — |
| Reactant | Benzonitrile, 4-(trifluoromethyl)- | HCID 67995 | — |
| Reactant | 5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazole | HCID 23073221 | — |
| Reactant | HCID 58968618 | HCID 58968618 | — |
| Product | HCID 58968667 | HCID 58968667 | — |
Reaction Steps
1-(2-(((3,5-bis(trifluoromethyl)benzyl)(2-methyl-2H-tetrazol-5-yl)amino)methyl)-4-(trifluoromethyl)phenyl)-2-cyclopentylethanol was converted to the methyl ether with methyl iodide using a procedure analogous to that used for the preparation of N-(2-(cyclohexyl(methoxy)methyl)-5-trifluoromethyl)benzyl)-N-(3,5-bis(trifluoromethyl)benzyl)-2-methyl-2H-tetrazol-5-amine. LC-MS Calc. 609.5, found 610.5 (M+H). Examples 71-73 were prepared by an analogous series of reactions from 2-((3,5-bis(trifluoromethyl)benzyl)(2-methyl-2H-tetrazole-5-yl)amino)methyl)-4-(trifluoromethyl)benzonitrile using the appropriate Grignard reagent and alkylating agent
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919506B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-bc5e3b09ae1f4323ad19619a0ce68736 |
| Source note | uspto-grants-2011_04 |