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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095398Generated: October 31, 2026

Triethylamine → HCID 57989572, compound

https://huagongshe.com/reaction/1095398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 18709502HCID 18709502—
ReactantHCID 57436051HCID 57436051—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 57989572HCID 5798957283%

Reaction Steps

To a solution of 7-methyl-1-[2-(methylthio)ethyl]-1,3-dihydro-2H-benzimidazol-2-one (0.21 g, 0.93 mmol) in 1,2-dichloroethane (5 mL) were added triethylamine (0.43 mL, 3.1 mmol) and 4-nitrophenyl chloroformate (0.23 g, 1.1 mmol) at 0° C. and the mixture was stirred at rt for 4 h. Then to this mixture was added a solution of N,N-dimethyl-tert-leucinamide (ca. 1.4 mmol, prepared according to the procedure described in steps 1 and 2 of example 3 from dimethylamine hydrochloride) in 1,2-dichloroethane (3 mL) at 0° C. and stirred rt. After 14 h, the reaction was quenched by addition of water (50 mL) and extracted with dichloromethane (50 mL×2). The combined organic layers were washed with water (30 mL×4), brine (30 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by preparative TLC eluting with dichloromethane/methanol (10/1) to afford 0.31 g (83%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138177B2
Source datasetuspto-grants-2012_03
ORD IDord-93d37480e0a7432990a4151e8b09d47d
Source noteuspto-grants-2012_03