HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 58980909, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 1-methyl-1H-imidazole-4-sulfonamide | HCID 2736885 | — |
| Reactant | HCID 69429123 | HCID 69429123 | — |
| Product | HCID 58980909 | HCID 58980909 | — |
Reaction Steps
Step A) Preparation of N-[tert-butyl(dimethyl)silyl]-1-methyl-1H-imidazole-4-sulfonamide: A mixture of 2.2 g (14 mmol) 1-methyl-1H-imidazole-4-sulfonamide, 2.1 g (14 mmol) t-butyldimethylsilyl chloride and 3.9 mL (28 mmol) triethylamine in 15 mL DMF was stirred at room temperature overnight Solvent was removed, and the residue was dissolved in EtOAc before being washed with water and brine. Drying (MgSO4) and removal of solvent gave 3 g of the subtitle product as a white solid, 1H NMR (DMSO) δ 7.7 (s, 1H), 7.6 (s, 1H), 7.35 (s, 1H), 3.7 (s, 3H), 0.9 (s, 9H)., 0.2 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285558B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-721bac0bd11448f98c29465f9abf2cb4 |
| Source note | uspto-grants-2007_10 |