HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenesulfonamide → HCID 67998722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenesulfonamide | HCID 72881 | — |
| Reactant | 5-Chlorothiophene-2-Sulfonamide | HCID 1241301 | — |
| Reactant | HCID 67999735 | HCID 67999735 | — |
| Product | HCID 67998722 | HCID 67998722 | — |
Reaction Steps
The title compound was prepared from methyl 2-((3R,5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((S)-1-cyclopropyl-2-hydroxyethyl)-3-methyl-2-oxopiperidin-3-yl)acetate (Example 263, Step C) by procedures similar to those described in Example 263, Step D and E, substituting thiophene-2-sulfonamide in Step D with the appropriate amount of 5-chlorothiophene-2-sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296736B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-12465dba5ba34c48bba0b4ef18bae1df |
| Source note | uspto-grants-2016_03 |