HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2-Chloro-4-methyl-1,3-thiazole-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Chloro-4-methyl-1,3-thiazole-5-sulfonyl chloride | HCID 12094250 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Chloro-4-methyl-1,3-thiazole-5-sulfonamide | HCID 12094251 | — |
Reaction Steps
A solution of 2-chloro-4-methylthiazole-5-sulfonyl chloride (1.0 g) in isopropyl alcohol (10 mL) was cooled with an ice-bath. Then, ammonium hydroxide (2.89 ml) was added slowly. The resulting solution was stirred at ambient temperature overnight. The solution was concentrated, the residue was mixed with water (10 mL) and extracted with ethyl acetate (2×20 mL). The crude product was purified on a silica gel column eluting with 60% ethyl acetate-hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156856B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-eef337d5ecf64eb3b62c4f3853101dd8 |
| Source note | uspto-grants-2015_10 |