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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596812Generated: October 25, 2026

N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine amide → N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine n-propylamide

https://huagongshe.com/reaction/596812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine amideHCID 22796331—
ReactantL-methionyl-L-aspartyl-D-alanine n-propylamide hydrochlorideHCID 22796356—
ProductN-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine n-propylamideHCID 22796332—

Reaction Steps

When an equivalent quantity of L-methionyl-L-aspartyl-D-alanine n-propylamide hydrochloride is substituted for the L-methionyl-L-aspartyl-D-alanine amide hydrochloride of Example 6, and the procedure detailed therein substantially repeated, there is obtained N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine n-propylamide. This compound melts at about 143.5°-148° C. with decomposition and is represented by the following formula.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012367
Source datasetuspto-grants-1977_03
ORD IDord-7c2617dbcc114a10ab5bb5e45f67f47f
Source noteuspto-grants-1977_03