HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200083Generated: October 31, 2026
Diisopropylethylamine → HCID 76072182, compound
https://huagongshe.com/reaction/2200083
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 1259362 | HCID 1259362 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 62648620 | HCID 62648620 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 76072182 | HCID 76072182 | 18% |
Reaction Steps
A solution of crude [1-(4-trifluoromethyl-phenyl)-piperidin-3-yl]-methylamine (30.0 mg, 0.12 mmol, crude) and [ethyl-(4-fluoro-benzenesulfonyl)-amino]-acetic acid (30.0 mg, 0.12 mmol) in dichloromethane (5 mL) at 25° C. was treated with HATU (43.7 mg, 0.12 mmol). N,N-Diisopropylethylamine (29.7 mg, 0.23 mmol) was added to the solution. The reaction mixture was stirred for 2 h. The reaction mixture was then poured into 0.2 M aqueous KHSO4 solution and extracted three times with ethyl acetate. The combined organic layers were washed three times with water and once with brine. The organic layer was then dried over magnesium sulfate, filtered and concentrated in vacuo. Flash column chromatography (50/50 hexanes/ethyl acetate) afforded 2-[ethyl-(4-fluoro-benzenesulfonyl)-amino]-N-[1-(4-trifluoromethyl-phenyl)-piperidin-3-ylmethyl]-acetamide (10.2 mg, 18%) as a white solid. [MH]+=502.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09359337B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-da887bc16a194689a69d775090eaf905 |
|---|
| Source note | uspto-grants-2016_06 |
|---|