HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → butyl (S)-2-(2-benzoylphenylamino)-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Carbodiimide | HCID 160435 | — |
| Reactant | (S)-2-(2-benzoylphenylamino)-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl)propionic acid | HCID 10483579 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | butyl (S)-2-(2-benzoylphenylamino)-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl]propionate | HCID 11764815 | 20.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807669B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-e25a0a5ae9ce40e8a8717d1c6a53f6ca |
| Source note | uspto-grants-2010_10 |