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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189913Generated: October 29, 2026

Aniline → HCID 11066741, compound

https://huagongshe.com/reaction/1189913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantL-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11066741HCID 1106674144.3%

Reaction Steps

8.43 g (44.0 mmol) of EDCl was added to 100 ml of THF solution of 9.97 g (40.0 mmol) of Boc-Leu-OH (manufactured by Tokyo Chemical Industry Co., Ltd), 3.65 ml (40.0 mmol) of aniline and 4.60 g (40.0 mmol) of HO-Su(hydroxysuccinimide), followed by stirring for 8 hours at room temperature. After a reaction mixture was concentrated under reduced pressure, the concentrate was extracted by adding water and ethyl acetate. After an organic layer was washed sequentially with a diluted hydrochloric acid, an aqueous solution of sodium hydrogen carbonate and water (one time for each), the organic layer was dried over sodium sulfate. After the drying agent was separated by filtration, the filtrate was concentrated under reduced pressure, thereby obtaining crude amide. The obtained amide compound was purified by a silica gel column chromatography (hexane/ethyl acetate=9/1 to 2/1 (volume ratio)), thereby obtaining 5.43 g of the product with a yield of 44.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674144B2
Source datasetuspto-grants-2014_03
ORD IDord-049b723b6b23494ebd1eaefba96f72ce
Source noteuspto-grants-2014_03