HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 5-sulfonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | (R)-5-Amino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole | HCID 10376533 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-sulfonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole | HCID 19970255 | — |
| Product | 5-carbonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole | HCID 86749715 | — |
Reaction Steps
To a stirred solution of (R)-5-amino-3-(N-methylpyrrolidin-2-ylmethyl)indole (0.229 g, 1.00 mmol) and triethylamine (0.21 mL, 1.5 mmol, 1.5 eq) in anhydrous acetonitrile (3 mL) at 0° C. under nitrogen was added the appropriate carbonyl chloride or sulfonyl chloride (1.5 mmol, 1.5 eq). The resulting reaction mixture was stirred at room temperature for 12 hours. The reaction mixture was then evaporated under reduced pressure, and the residue was column chromatographed using silica gel (approximately 25 g) and elution with an appropriate solvent system afforded the appropriate 5-carbonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole or 5-sulfonylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559129 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-ff2688cae71f41ac874a4027683f8001 |
| Source note | uspto-grants-1996_09 |