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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347898Generated: November 1, 2026

Diisopropylethylamine → HCID 11696413, compound

https://huagongshe.com/reaction/347898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant3-IsocyanatopyridineHCID 2760493—
ReactantHCID 68983099HCID 68983099—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 11696413HCID 11696413—

Reaction Conditions

Temperature10 °C

Reaction Steps

A 22 L 3-neck RBF equipped with a cooling bath, mechanical stirrer, thermocouple, and nitrogen bubbler was purged with nitrogen for at least ten minutes. The flask was charged with 1.441 kg (4.990 mol) 1-[(R)-3-(3-amino-5-fluoro-phenoxy)-piperidin-1-yl]-ethanone HCl salt and 14.4 L (10 vol) dichloromethane. The solution was stirred, and 0.710 kg (5.489 mol) DIPEA was charged. The solution was cooled to 10±5° C. in an ice/brine bath. The reaction was charged with 0.659 kg (5.489 mol) 3-isocyanato-pyridine and the solution warmed to room temperature and stirred for three hours. The reaction was monitored by TLC (1:9 methanol:ethyl acetate/PMA stain) and HPLC. The reaction stirred at room temperature for five more hours, and another 0.009 kg (0.075 mol) 3-isocyanato-pyridine was added. The solution stirred for 15 more hours, and the reaction was deemed complete. The solution was poured into a 50 L extractor containing 14.4 L (10 vol) saturated sodium bicarbonate, and the flask was rinsed with an additional 1.44 L (1 vol) dichloromethane. The layers were separated, and the organic layer was washed with 14.4 L (2×10 vol) water. The organic layer was dried with 1.69 kg sodium sulfate for at least 20 minutes before proceeding to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176222B2
Source datasetuspto-grants-2007_02
ORD IDord-c302b048e30b4883b2cbdf9efdfe8eff
Source noteuspto-grants-2007_02