HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → N-(Butylamino)carbonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3(4-Imidazol-1-ylmethylphenyl)5-iso-butylthiophene-2 sulfonamide | HCID 11394744 | — |
| Reactant | 3-(4-Imidazol-1-ylmethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide | HCID 11419042 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(Butylamino)carbonyl-3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonamide | HCID 10227337 | 33% |
Reaction Steps
The crude product from step (c) above was dissolved in acetone (5 mL) under N2 (g). NaOH (0.20 mL, 1M, 0.20 mmol) was added to the mixture, which was then stirred for 10 min. Butyl isocyanate (109 μL, 0.97 mmol) was then added and the mixture was stirred overnight at room temperature. The reaction mixture was then diluted with ethyl acetate (150 mL) and washed with water and brine. The organic phase was dried over MgSO4 and the solvent was removed in vacuo. Purification using column chromatography with CHCl3:MeOH (10:1) as eluent yielded the title compound (15.1 mg, 0.032 mmol) in 33% yield (from 3-(4-imidazol-1-ylmethylphenyl)-5-iso-butylthiophene-2-sulfonic acid tert-butylamide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124638B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-f349ccd448764fecb3e7ee660c57d58a |
| Source note | uspto-grants-2012_02 |