HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (R)-2-(1H-imidazole-1-sulfonamido)-4-methoxy-N,N,N-trimethyl-4-oxobutan-1-aminium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Imidazole-1-sulfonyl)-1-methyl-3H-imidazol-1-ium triflate | HCID 11728149 | — |
| Reactant | (R)-2-amino-4-methoxy-N,N,N-trimethyl-4-oxobutan-1-aminium chloride | HCID 86641220 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (R)-2-(1H-imidazole-1-sulfonamido)-4-methoxy-N,N,N-trimethyl-4-oxobutan-1-aminium chloride | HCID 68743870 | — |
Reaction Steps
A solution of (R)-2-amino-4-methoxy-N,N,N-trimethyl-4-oxobutan-1-aminium chloride (35 mg) in anhydrous MeCN (5 mL) is treated with triethyl amine (2.5 equiv.) and 3-(Imidazole-1-sulfonyl)-1-methyl-3H-imidazol-1-ium triflate (1.5 equiv.). The reaction mixture is stirred at ambient temperature for 16 h then concentrated under reduced pressure and the resulting residue is purified on silica gel using MeOH/DCM (0->80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410150B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-682aef7c5b9c4c7bb0e1857df13798f4 |
| Source note | uspto-grants-2013_04 |