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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666429Generated: October 27, 2026

Diisopropylethylamine → HCID 24965143, compound

https://huagongshe.com/reaction/1666429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Amino-2-methylpyridineHCID 243313—
ReactantPhenyl 6-methylpyridin-3-ylcarbamateHCID 54438385—
Reactant4-(3-(4-(Trifluoromethyl)phenoxy)benzylidene)piperidine hydrochlorideHCID 66875732—
SolventAcetonitrileHCID 6342—
ProductHCID 24965143HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-809ff8653dff4ef39d363cec21a3173b
Source noteuspto-grants-2011_10