HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic acid, 2-chloro-5-(chlorosulfonyl)- → Benzoic acid, 2-chloro-5-[(methylamino)sulfonyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic acid, 2-chloro-5-(chlorosulfonyl)- | HCID 67306 | — |
| Reactant | HCID 54433427 | HCID 54433427 | — |
| Product | Benzoic acid, 2-chloro-5-[(methylamino)sulfonyl]- | HCID 111724 | — |
| Product | Benzoic acid, 2-amino-5-[(methylamino)sulfonyl]- | HCID 122430 | — |
Reaction Steps
5-(N-Methylsulfamoyl)-isatoic anhydride, which is to be used as the starting material, can be obtained, for example, in a manner analogous to that described in Example 1, using 2-chloro-5-chlorosulfonyl-benzoic acid as the starting material, the product being obtained via 2-chloro-5-(N-methylsulfamoyl)-benzoic acid with a melting point of 170°-172° and 5-(N-methylsulfamoyl)-anthranilic acid with a melting point of 205°; the product melts at 260°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04505913 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-eb068a0a1aa6482d9f219f47fb2f2217 |
| Source note | uspto-grants-1985_03 |