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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254561Generated: November 1, 2026

2-(2-(Benzylcarbamoyl)-1-methylhydrazinyl)acetic acid → 4-benzyl-1-(2-((S)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1,4-dioxo-4-(tritylamino)butan-2-ylamino)-2-oxoethyl)-1-methylsemicarbazide

https://huagongshe.com/reaction/1254561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-(Benzylcarbamoyl)-1-methylhydrazinyl)acetic acidHCID 53397489—
Reactant(S)-2-amino-N1-((S)-1,1-diethoxypropan-2-yl)-N1-(quinolin-8-ylmethyl)-N4-tritylsuccinamideHCID 67075012—
Product4-benzyl-1-(2-((S)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1,4-dioxo-4-(tritylamino)butan-2-ylamino)-2-oxoethyl)-1-methylsemicarbazideHCID 67088390—

Reaction Steps

According to the procedure described in the synthesis method of Compound II-15, 2-(2-(benzylcarbamoyl)-1-methylhydrazinyl)acetic acid (Compound VI-3) 55 mg (0.23 mmol) was coupled with (S)-2-amino-N1—((S)-1,1-diethoxypropan-2-yl)-N1-(quinolin-8-ylmethyl)-N4-tritylsuccinamide (Compound IV-20) 100 mg (0.16 mmol) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455488B2
Source datasetuspto-grants-2013_06
ORD IDord-c88e804a55a44fcdb621bb20b5eb6a79
Source noteuspto-grants-2013_06