HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-Chloro-2-Methyl-6-Sulfamyl-1H-Benzimidazole Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4,5-Diamino-2-chlorobenzene-1-sulfonamide | HCID 13289688 | — |
| Product | 5-Chloro-2-Methyl-6-Sulfamyl-1H-Benzimidazole Hydrochloride | HCID 20477857 | — |
Reaction Steps
To 10 ml of 4 N hydrochloric acid containing 0.86 ml of acetic acid was added 2.22 g. of 2-amino-4-chloro-5-sulfamylaniline (VI) and the mixture refluxed for four hours. Concentration in vacuo gave a blue solid which was collected by filtration, dissolved in methanol, treated with charcoal and filtered. The blue solution was concentrated in vacuo and triturated with ether to yield a blue solid. Washing with methanol provided the product as light blue crystals which upon drying gave 1.0 g. of 5(6)-chloro-2-methyl-6(5)-sulfamyl-1(3)H-benzimidazole hydrochloride, m.p. 313°-316° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420487 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-98369326657942aca737b03fa8897ebb |
| Source note | uspto-grants-1983_12 |