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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157501Generated: October 30, 2026

1-Butanol → butyl (S)-2-(2-benzoylphenylamino)-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl]propionate

https://huagongshe.com/reaction/1157501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantCarbodiimideHCID 160435—
Reactant(S)-2-(2-benzoylphenylamino)-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl)propionic acidHCID 10483579—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Productbutyl (S)-2-(2-benzoylphenylamino)-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl]propionateHCID 1176481520.1%

Reaction Steps

4.7 mg (63.3 μmol) of n-butanol, 5.7 mg (8.5 μmol) of PS-DMAP resin and 68 mg (94.0 μmol) of PS-carbodiimide are added successively to a solution containing 25 mg (42.3 μmol) of (S)-2-(2-benzoylphenylamino)-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propionic acid (Example 2) in 0.6 ml of DCM. After stirring for 16 h at ambient temperature and then 5 h at 40° C., the reaction medium is filtered and the solvents are evaporated off. The reaction crude is purified by chromatography on a column of silica and eluted with a heptane/ethyl acetate mixture. 5.5 mg of butyl (S)-2-(2-benzoylphenylamino)-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propionate are obtained with a 20% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807669B2
Source datasetuspto-grants-2010_10
ORD IDord-e25a0a5ae9ce40e8a8717d1c6a53f6ca
Source noteuspto-grants-2010_10