HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747770Generated: October 29, 2026
Triethylamine → benzyl (3R)-4-(5-cyano-2-iodophenoxy)-3-(4-dimethylcarbamoylbenzoylamino)butyrate
https://huagongshe.com/reaction/747770
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-(Dimethylcarbamoyl)benzoic acid | HCID 11095480 | — |
| 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-dimethylcarbamoylbenzoylamino)butyrate | HCID 54212177 | — |
Reaction Steps
2.05 g (4.33 mmol) of (1R)-1-benzyloxycarbonylmethyl-2-(5-cyano-2-iodophenoxy)ethyl ammonium chloride, 1.25 g (6.49 mmol) of 4-dimethylcarbamoylbenzoic acid, 994 mg (7.35 mmol) of 1-hydroxybenzotriazole, and 2.71 ml (19.46 mmol) of triethylamine were dissolved in 25 ml of dichloromethane, and 1.41 g (7.35 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 to obtain the crude product. It was purified by silica gel column chromatography (hexane:ethyl acetate=3:1, v/v) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396844B1 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-558a342599224a5d8e323c80e519f1b9 |
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| Source note | uspto-grants-2008_07 |
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