HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518681Generated: October 27, 2026
Diisopropylethylamine → HCID 178457856, compound
https://huagongshe.com/reaction/518681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(2-(3-Fluoro-4-nitrophenoxy)ethyl)piperidine | HCID 66728447 | — |
| Reactant | HCID 178457872 | HCID 178457872 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178457856 | HCID 178457856 | — |
Reaction Steps
To a solution of 1-(2-(3-fluoro-4-nitrophenoxy)ethyl)piperidine (220 mg, 0.820 mmol) and cis-4-amino-N-isopropylcyclohexanecarboxamide hydrochloride (190 mg, 0.861 mmol) in ACN (0.8 mL) was added DIPEA (0.301 mL, 1.722 mmol). The mixture was heated at 80° C. in a sealed tube for 14 hours, and then additional cis-4-amino-N-isopropylcyclohexanecarboxamide hydrochloride (38 mg, 0.172 mmol) and DIPEA (0.100 mL, 0.574 mmol) were added. The resulting mixture was heated an additional 24 hours. The mixture was diluted with DCM (5 mL), washed with water/brine mixture, brine, and the organic layer was dried over Na2SO4, filtered and evaporated to afford cis-N-isopropyl-4-(2-nitro-5-(2-(piperidin-1-yl)ethoxy)phenylamino)cyclohexanecarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115127B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-f7db9cb14e984deb8ecc85888c7df7bb |
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| Source note | uspto-grants-2015_08 |
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