HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyryl chloride → HCID 59656379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 11750377 | HCID 11750377 | — |
| Product | HCID 59656379 | HCID 59656379 | — |
Reaction Steps
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-1-carboxylic acid (2-chloro-phenyl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-1-carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chlorformate. Wt.: 21 mg (27%). 1H NMR (300 MHz, CDCl3) δ 8.67 (m, 2H), 8.48 (d, 1H), 8.35 (d, 1H), 8.20 (s, 1H), 7.82 (d, 1H), 7.72 (m, 2H), 7.41 (m, 2H), 7.09 (m, 1H), 4.78 (d, 1H), 4.31 (m, 1H), 3.67 (m, 1H), 3.35 (m, 1H), 2.95 (m, 1H), 2.22 (m, 2H), 1.60 (4H), 1.27 (m, 2H), 0.92 (t, 3H); LC/MS m/z 515 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063222B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-0dc7b8868a9045aa9a33fa7065854f05 |
| Source note | uspto-grants-2011_11 |