HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → benzyl (3R)-4-(5-cyano-2-iodophenoxy)-3-[4-(pyrrolidine-1-carbonyl)benzoylamino]butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (1R)-1-benzyloxycarbonylmethyl-2-(5-cyano-2-iodophenoxy)ethylammonium chloride | HCID 86760714 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl (3R)-4-(5-cyano-2-iodophenoxy)-3-[4-(pyrrolidine-1-carbonyl)benzoylamino]butyrate | HCID 86760715 | — |
Reaction Steps
2.0 g (4.23 mmol) of (1R)-1-benzyloxycarbonylmethyl-2-(5-cyano-2-iodophenoxy)ethyl ammonium chloride, 1.02 g (4.65 mmol) of 4-pyrrolidine-1-carbonyl)benzoic acid, 630 mg (4.65 mmol) of 1-hydroxybenzotriazole, and 1.30 ml (9.31 mmol) of triethylamine were dissolved in 40 ml of dichloromethane, and 890 mg (4.65 mmol) of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride was added thereto and stirred under cooling with ice for 10 minutes and then at room temperature for 18 hours. The reaction was stopped by adding water, and the title compound was obtained in an ordinary manner by treatment with dichloromethane as the extractant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396844B1 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-668648b39abc4945a20eb03e2dccf5a3 |
| Source note | uspto-grants-2008_07 |