Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895506Generated: October 27, 2026

1,2-Dichloroethane → 7-Methyl-2-propyl-3H-benzoimidazole-5-carboxylic acid ((R)-1-benzyl-2-benzyloxycarbamoylethyl)amide

https://huagongshe.com/reaction/1895506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant7-Methyl-2-propyl-1H-benzimidazole-5-carboxylic acidHCID 10262831—
Reactant(R)-3-amino-N-benzyloxy-4-phenylbutyramideHCID 14134575—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product7-Methyl-2-propyl-3H-benzoimidazole-5-carboxylic acid ((R)-1-benzyl-2-benzyloxycarbamoylethyl)amideHCID 4415846141.2%

Reaction Steps

To a solution of 7-methyl-2-propyl-3H-benzoimidazole-5-carboxylic acid (164 mg, 752 μmol) and (R)-3-amino-N-benzyloxy-4-phenylbutyramide (TFA salt: 300 mg, 754 μmol) in DMF (10 mL) containing triethylamine (210 μL), was added HOBt (151 μg, 755 μmol) and EDC (151 mg, 788 μmol). The mixture was stirred at room temperature overnight and concentrated in vacuo, yielding a pale brown residue. The residue was dissolved in DCM (100 mL) and washed sequentially with 1M H3PO4, a saturated NaHCO3 solution, and saturated aqueous NaCl. The organic layer was collected, dried over MgSO4, and concentrated to afford the title compound as a pale yellow oil (150 mg; 41% yield), which was used without further treatment. ESMS [M+H]+ calcd for C29H32N4O3, 485.26. found 485.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513432B2
Source datasetuspto-grants-2013_08
ORD IDord-721f8970b16c4ad4b65d0d424f16a83b
Source noteuspto-grants-2013_08