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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400038Generated: November 3, 2026

Triethylamine → HCID 49853919, compound

https://huagongshe.com/reaction/1400038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 67515007HCID 67515007—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 49853919HCID 4985391940.2%

Reaction Steps

To a stirred solution of hydrochloride salt of N-{3-[4-(3-aza-bicyclo[3.1.0]hex-1-yl)-phenyl]-2-oxo-oxazolidin-5(S)-yl-methyl}-acetamide (Intermediate IV) (210 mg, 0.6 mmol), in dichloroethane (25 mL), were added 3-pyridinecarboxaldehyde (0.06 mL, 0.6 mmol), triethyl amine (0.17 mL, 1.2 mmol) and sodium triacetoxyborohydride (254 mg, 1.2 mmol) at 0° C. under nitrogen atmosphere. The reaction mixture was stirred at r.t. and progress of the reaction was monitored by TLC. On completion, the reaction mixture was quenched by adding saturated aq. NaHCO3 solution (20 mL) and product was extracted with DCM (3×25 mL). The organic layer was washed with water (25 mL), brine (25 mL), dried over anhydrous sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (silica gel, 0.5:9.5 MeOH:CHCl3) to provide the title compound (98 mg, 40%) as off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906913B2
Source datasetuspto-grants-2014_12
ORD IDord-e3bdee561a854a85a5b1f9f23d5af5f9
Source noteuspto-grants-2014_12