HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467880Generated: November 2, 2026
Diisopropylethylamine → HCID 57664570, compound
https://huagongshe.com/reaction/1467880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Butoxybenzenesulfonyl Chloride | HCID 517990 | — |
| Reactant | N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamide | HCID 2773944 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57664570 | HCID 57664570 | 25% |
Reaction Steps
150 mg (0.434 mmol) of N-cyclopropyl-N-piperidin-4-yl-3-trifluoromethylbenzenesulfonamide (available from Lancaster) and 108 mg (0.434 mmol) of 4-butoxyphenylsulfonyl chloride (available from Matrix Scientific) were each dissolved in 10 mL of DCM and then combined. 1.5 eq. of DIEA (0.113 mL) was added to the mixture by syringe. The mixture was stirred overnight at room temperature and then concentrated under vacuum. The resultant product 29 was purified through a column of silica gel with a gradient of 0% to 20% EtOAc in hexanes and the pure material was concentrated (yield 25%, white solid). 1H NMR (CDCl3): δ 8.058 (s, 1H), 8.003-7.983 (d, 1H), 7.851-7.831 (d, 1H), 7.688-7.641 (m, 3H), 7.017-6.980 (m, 2H), 4.055-4.022 (t, 2H), 3.843-3.746 (m, 3H), 2.286-2.226 (t, 2H), 2.068-1.901 (m, 3H), 1.843-1.773 (m, 2H), 1.6151-1.470 (m, 4H), 1.014-0.976 (t, 3H), 0.944-0.903 (m, 2H), 0.793-0.744 (m, 2H). LC: 100%. MS (e/z): 562 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09000174B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-02f1a3d68a684ad98ecadb5e6fa1ab1e |
|---|
| Source note | uspto-grants-2015_04 |
|---|