HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666429Generated: October 27, 2026
Diisopropylethylamine → HCID 24965143, compound
https://huagongshe.com/reaction/1666429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Amino-2-methylpyridine | HCID 243313 | — |
| Reactant | Phenyl 6-methylpyridin-3-ylcarbamate | HCID 54438385 | — |
| Reactant | 4-(3-(4-(Trifluoromethyl)phenoxy)benzylidene)piperidine hydrochloride | HCID 66875732 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 24965143 | HCID 24965143 | — |
Reaction Steps
4-(3-(4-(Trifluoromethyl)phenoxy)benzylidene)piperidine hydrochloride (200 mg, 0.541 mmol, from Example 53, Step 5) and phenyl 6-methylpyridin-3-ylcarbamate (123 mg, 0.541 mmol, prepared according to the procedure described in Synthesis, 1997, 1189-1194 from 3-amino-6-methylpyridine) and diisopropylethylamine (0.20 mL, 1.15 mmol) were combined in acetonitrile (5 mL) and stirred at room temperature. After 16 h, the reaction was concentrated and the residue was purified by silica gel chromatography (50-100% EtOAc:CH2Cl2) to afford the title compound (220 mg) as a white solid. MS APCI M+ 468.2, 375.2, 334.1 M− 466.1; 1H NMR (400 MHz, CD3OD) δ ppm 2.41-2.45 (m, 2H) 2.46 (s, 3H) 2.54 (td, J=5.90, 1.26 Hz, 2H) 3.50-3.55 (m, 2H) 3.58-3.65 (m, 2H) 6.43 (s, 1H) 6.91-6.96 (m, 2H) 7.06-7.12 (m, 3H) 7.20 (d, J=8.52 Hz, 1H) 7.35-7.42 (m, 1H) 7.59-7.68 (m, 2H) 7.77 (dd, J=8.45, 2.62 Hz, 1H) 8.43 (d, J=2.78 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044052B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-809ff8653dff4ef39d363cec21a3173b |
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| Source note | uspto-grants-2011_10 |
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