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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431812Generated: October 25, 2026

Decanoic Acid → N-alpha-decyl-L-phenylalanine 2-aminopyridine

https://huagongshe.com/reaction/431812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecanoic AcidHCID 2969—
ReactantDicyclohexylcarbodiimideHCID 10868—
ProductN-alpha-decyl-L-phenylalanine 2-aminopyridineHCID 69929295—

Reaction Steps

The acylated phenylalanine anilide imprint molecule was synthesized in three steps. (1) N-α-t-BOC-L-phenylalanine was coupled with 2-aminopyridine using DCC to give N-α-t-BOC-L-phenylalaniine-2-aminopyridine. (2) The a-amine was then deprotected with TFA to give N-α-L-phenylalanine-2-aminopyridine. (3) To create a compound having the properties of a surfactant, the free amine was then acylated with decanoic acid using DCC to give N-α-decyl-L-phenylalanine-2-aminopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660780B2
Source datasetuspto-grants-2003_12
ORD IDord-4eddb75f7dab42a693198cb7ff2c3dcd
Source noteuspto-grants-2003_12