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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N-((1,1-dimethylethoxy)carbonyl)-2-methyl-alanine | HCID 2733845 | — |
| Reactant | (S)-2-Amino-3-(1H-indol-3-yl)-N-phenylpropanamide | HCID 16735217 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-Aib-Trp-NHPh | HCID 90045880 | 65.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674144B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-2a5c6a0635984dfc809e2df8ad4e0eee |
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| Source note | uspto-grants-2014_03 |
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