HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-cyanomethoxyphenyl)methanesulfonamide → N-(3-chloro-5-cyanomethyl-2-methylphenyl) methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-cyanomethoxyphenyl)methanesulfonamide | HCID 18789601 | — |
| Reactant | 2-(3-Aminophenoxy)acetonitrile | HCID 18789699 | — |
| Reactant | (3-Amino-5-chloro-4-methylphenyl) acetonitrile | HCID 54396229 | — |
| Product | N-(3-chloro-5-cyanomethyl-2-methylphenyl) methanesulfonamide | HCID 53903521 | — |
Reaction Steps
N-(3-chloro-5-cyanomethyl-2-methylphenyl) methanesulfonamide was prepared from (3-amino-5-chloro-4-methylphenyl) acetonitrile in a manner similar to that described in Example 1 for the preparation of N-(3-cyanomethoxyphenyl)-methanesulfonamide from (3-aminophenoxy)-acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057349 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-a2c6a46cfcde4a0e9df01dc3b8088c77 |
| Source note | uspto-grants-2000_05 |