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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482468Generated: October 30, 2026

Triethylamine → 3-Phenylpropanamide

https://huagongshe.com/reaction/482468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantBoc-D-phenylalanineHCID 637610—
Reactant3-Amino-1,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-1,4-benzodiazepin-2-oneHCID 15379622—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-PhenylpropanamideHCID 7625—

Reaction Conditions

Temperature5 °C

Reaction Steps

1.73 g of 3-amino-1,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-1,4-benzodiazepin-2-one are dissolved in 30 ml of dimethylformamide in the presence of 1.42 g of BOC-D-phenylalanine, followed by cooling to 5° C. and addition of 1.07 ml of triethylamine and then 2.4 g of BOP. The reaction mixture is allowed to return to room temperature and is left stirring overnight. It is then poured into water and extracted with ethyl acetate. The organic phase is washed with water, separated out after settling of the phases, dried over Na2SO4, filtered and concentrated under vacuum. An oily residue of 2-tertbutoxycarbonylamino-N-]2,3-dihydro-5-(2,6-dimethoxy-4-methylphenyl)-1-methyl-2-oxo-1H-1,4-benzodiazepin-3-yl!-3-phenylpropionamide, obtained in quantitative yield, is used as it is for the following step (Compound 16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798353
Source datasetuspto-grants-1998_08
ORD IDord-2b7eac7a0dc0463ba47799a4d8789f96
Source noteuspto-grants-1998_08