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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189916Generated: November 1, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → Boc-Aib-Trp-NHPh

https://huagongshe.com/reaction/1189916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-((1,1-dimethylethoxy)carbonyl)-2-methyl-alanineHCID 2733845—
Reactant(S)-2-Amino-3-(1H-indol-3-yl)-N-phenylpropanamideHCID 16735217—
SolventTetrahydrofuranHCID 8028—
ProductBoc-Aib-Trp-NHPhHCID 9004588065.3%

Reaction Steps

2.78 g (14.5 mmol) of EDCl was added to 40 ml of THF solution of 1.47 g (7.25 mmol) of Boc-Aib-OH (manufactured by Sigma-Aldrich Corporation), and 2.03 g (7.25 mmol) of H-Trp-NHPh obtained in Synthesis Example 4-2, followed by stirring for 16 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), it was concentrated under reduced pressure, thereby obtaining crude amide. The obtained amide compound was purified by a silica gel column chromatography (hexane/ethyl acetate=3/1 to 0/1 (volume ratio)), thereby obtaining 2.20 g of the product with a yield of 65.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674144B2
Source datasetuspto-grants-2014_03
ORD IDord-2a5c6a0635984dfc809e2df8ad4e0eee
Source noteuspto-grants-2014_03