HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200084Generated: November 1, 2026
Diisopropylethylamine → HCID 76072183, compound
https://huagongshe.com/reaction/2200084
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| 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 | 2-[N-(propan-2-yl)4-fluorobenzenesulfonamido]acetic acid | HCID 60827977 | — |
| Reactant | HCID 62648620 | HCID 62648620 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 76072183 | HCID 76072183 | 53.9% |
Reaction Steps
A solution of crude [1-(4-trifluoromethyl-phenyl)-piperidin-3-yl]-methylamine (47.0 mg, 0.18 mmol, crude) and [(4-fluoro-benzenesulfonyl)-isopropyl-amino]-acetic acid (50.0 mg, 0.18 mmol) in dichloromethane (5 mL) at 25° C. was treated with HATU (69.1 mg, 0.18 mmol). N,N-Diisopropylethylamine (46.9 mg, 0.36 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 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-[(4-fluoro-benzenesulfonyl)-isopropyl-amino]-N-[1-(4-trifluoromethyl-phenyl)-piperidin-3-ylmethyl]-acetamide (50.0 mg, 53%) as a white solid. [MH]+=516.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359337B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-ac7c00736f2c44df92cabf657e5ee972 |
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| Source note | uspto-grants-2016_06 |
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