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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878693Generated: October 31, 2026

Triethylamine → HCID 25018141, compound

https://huagongshe.com/reaction/1878693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 25018139HCID 25018139—
SolventDichloromethaneHCID 6344—
ProductHCID 25018141HCID 2501814170.1%

Reaction Steps

To a solution of 5-(3-amino-4-methylphenyl)-1-(2-(7-methoxyquinolin-4-yloxy)ethyl)pyridin-2(1H)-one (0.10 g, 0.25 mmol) in 10 mL of CH2Cl2 at rt was added triethylamine (0.083 ml, 0.60 mmol) followed by isobutyl chlorocarbonate (0.048 ml, 0.37 mmol). The reaction was stirred at rt for 4 hours and was then concentrated in vacuo. The residue was dissolved in 50 mL of EtOAc and the resulted organic phase was washed with 20 mL of satd. NaHCO3 followed by 20 mL of brine. The organic solution was dried over Na2SO4 and concentrated in vacuo. The residue was washed with 50% hex/EtOAc to give white solid as desired product (0.0879 g, 70% yield). MS (ESI pos. ion) m/z (MH+): 502.1. Calc'd Exact Mass for C29H31N3O5: 501.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314087B2
Source datasetuspto-grants-2012_11
ORD IDord-7b6777946ebb4fefb1d55e544a38fe76
Source noteuspto-grants-2012_11