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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303362Generated: November 1, 2026

N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-alanine → N-[2-(tert-butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-Nalpha-(9-fluorenylmethoxycarbonyl)-L-alanine amide

https://huagongshe.com/reaction/2303362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-alanineHCID 6364642—
ReactantN-[2-(tert-butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amineHCID 18460594—
ProductN-[2-(tert-butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-Nalpha-(9-fluorenylmethoxycarbonyl)-L-alanine amideHCID 86758402—

Reaction Steps

N-[2-(tert-Butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amine (756 mg) and N-(9-fluorenylmethoxycarbonyl)-L-alanine (544 mg) were treated in the same manner as in Preparation Example 9 to obtain the title compound. Since this compound was unable to be isolated from impurities, it was used in the next reaction without purifying it as it is.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432957B1
Source datasetuspto-grants-2002_08
ORD IDord-e66b1104d77c49c6b953eb064b635d3f
Source noteuspto-grants-2002_08