HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 13138216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20455856 | HCID 20455856 | — |
| Product | HCID 13138216 | HCID 13138216 | — |
| Product | 5-acetamido-2-chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesulfonamide | HCID 20455858 | — |
Reaction Steps
To a solution of 37.3 g of 5-amino-2-chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesulfonamide prepared in a minimum amount of boiling chloroform, is added with vigorous stirring 20.4 g of acetic anhydride. The resulting mixture is then refluxed for 2 hours, the chloroform, excess acetic anhydride and acetic acid are removed in vacuo to yield as residue the desired product, 5-acetamido-2-chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225337 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-536633c1244a4c5e848efc64e2884d0c |
| Source note | uspto-grants-1980_09 |