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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095395Generated: October 26, 2026

Triethylamine → PF-03550096

https://huagongshe.com/reaction/1095395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant(2S)-2-Amino-3,3-dimethylbutanamideHCID 11297986—
ReactantHCID 57436050HCID 57436050—
Solvent1,2-DichloroethaneHCID 11—
ProductPF-03550096HCID 2485788733.8%

Reaction Steps

To a solution of 1-(3-hydroxy-3-methylbutyl)-1,3-dihydro-2H-benzimidazol-2-one (0.25 g, 1.1 mmol) in 1,2-dichloroethane (30 mL) were added triethylamine (0.52 mL, 3.7 mmol) and 4-nitrophenyl chloroformate (0.27 g, 1.4 mmol) at 0° C. and the mixture was stirred for 4 h at rt. Then to this mixture was added a mixture of L-tert-leucinamide (0.18 g, 1.4 mmol) in 1,2-dichloroethane (5 mL) at 0° C. and stirred at rt. After 14 h, the reaction was quenched by addition of water (50 mL) and filtered and washed with water (30 mL) and dichloromethane (30 mL). The obtained solid was suspended in water (50 mL) and filtered. This procedure was repeated twice followed by recrystallization from methanol. The obtained solid was suspended in water (50 mL) again and filtered and this procedure was repeated twice. Then the solid was dissolved in methanol/dichloromethane and filtered and concentrated in vacuo. The obtained solid was then recrystallized from acetone to give 0.14 g (33%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138177B2
Source datasetuspto-grants-2012_03
ORD IDord-3d637b612c864fb2990391ee8f121f34
Source noteuspto-grants-2012_03