HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyryl chloride → HCID 59656453, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 11750377 | HCID 11750377 | — |
| Product | HCID 59656453 | HCID 59656453 | — |
Reaction Steps
The title compound was prepared according to the general procedure in Scheme 11, substituting 4-(piperidin-4-ylsulfamoyl)-naphthalene-1-carboxylic acid (tetrahydro-pyran-4-yl)-amide for 4-(piperidin-4-ylsulfamoyl)-naphthalene-1-carboxylic acid cyclohexylamide, and butyryl chloride for ethyl chloroformate. Wt.: 30 mg (19%). 1H NMR (300 MHz, CDCl3) δ 8.67 (d, 1H), 8.26 (d, 1H), 8.13 (d, 1H), 7.67 (m, 2H), 7.52 (d, 1H), 6.68 (m, 1H), 5.28 (m, 1H), 4.32 (m, 1H), 4.05 (m, 3H), 3.15 (m, 1H), 2.46 (m, 1H), 2.10 (m, 4H), 1.65 (m, 4H), 1.49 (m, 2H), 1.18 (m, 1H), 9.95 (m, 1H), 0.88 (t, 3H); LC/MS m/z 488 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329755B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-3f04a5515d7348009e737db9eb39e17b |
| Source note | uspto-grants-2008_02 |