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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254542Generated: November 2, 2026

2-(2-(Ethylcarbamoyl)-1-methylhydrazinyl)acetic acid → (S)-tert-butyl 4-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-3-(2-(2-(ethylcarbamoyl)-1-methylhydrazinyl)acetamido)-4-oxobutanoate

https://huagongshe.com/reaction/1254542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-(Ethylcarbamoyl)-1-methylhydrazinyl)acetic acidHCID 53397417—
Reactant(S)-tert-butyl 3-amino-4-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-4-oxobutanoateHCID 67075348—
Product(S)-tert-butyl 4-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-3-(2-(2-(ethylcarbamoyl)-1-methylhydrazinyl)acetamido)-4-oxobutanoateHCID 67088272—

Reaction Steps

According to the procedure described in the synthesis method of Compound II-15, 2-(2-(ethylcarbamoyl)-1-methylhydrazinyl)acetic acid (Compound VI-9) 57 mg (0.33 mmol) was coupled with (S)-tert-butyl 3-amino-4-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-4-oxobutanoate (Compound IV-16) 100 mg (0.22 mmol) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455488B2
Source datasetuspto-grants-2013_06
ORD IDord-fdeba863c6e04051851146875ab8b3c0
Source noteuspto-grants-2013_06