HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzyloxybenzhydrol → N-Isopropyl-3-(4-benzyloxybenzhydryl)indole-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzyloxybenzhydrol | HCID 10589580 | — |
| Reactant | N-isopropylindole-2-sulfonamide | HCID 54122335 | — |
| Product | N-Isopropyl-3-(4-benzyloxybenzhydryl)indole-2-sulfonamide | HCID 54062511 | 84.3% |
Reaction Steps
Substantially the same procedure as in Example 266 was repeated using 4-benzyloxybenzhydrol (1.31 g, 4.50 mmol) and N-isopropylindole-2-sulfonamide (1.00 g, 4.46 mmol) to give 1.92 g (yield: 84%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891902 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-4432879dce0e4b8782fe658f67423b6b |
| Source note | uspto-grants-1999_04 |