HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2,4-Dibromothiazole-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2,4-Dibromothiazole-5-sulfonyl chloride | HCID 86667482 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Dibromothiazole-5-sulfonamide | HCID 66748287 | 57% |
Reaction Steps
To a mixture of 2,4-dibromothiazole-5-sulfonyl chloride (3.17 g, 9.28 mmol) in THF (51.4 mL) was added 33% aqueous NH4OH (24.1 mL, 278 mmol) and the reaction was stirred at room temperature for 30 minutes. The reaction was concentrated in vacuo and the residue was taken up in ethyl acetate (100 mL) and water (100 mL). The aqueous layer was extracted with ethyl acetate (50 mL) and the combined organic layers were washed with water (50 mL) and brine (50 mL), then dried and concentrated in vacuo. The residue was purified by silica gel chromatography (ethyl acetate/DCM=0/100→20/80) to give 1.7 g (57% yield) of the title compound. as a white solid. LC/MS (FA) ES+ 321, 323, 325. 1H NMR (400 MHz, DMSO-d6) δ: 8.33 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796271B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-20aba556d99b47e0848d423042599bb1 |
| Source note | uspto-grants-2014_08 |