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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718935Generated: October 25, 2026

(S)-2-amino-3-(4-tert-butoxyphenyl)-N-((S)-1,1-diethoxypropan-2-yl)-N-(quinolin-8-ylmethyl)propanamide → 2-allyl-2-(2-((S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1-oxopropan-2-ylamino)-2-oxoethyl)-N-((S)-1-phenylethyl)hydrazinecarboxamide

https://huagongshe.com/reaction/718935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-amino-3-(4-tert-butoxyphenyl)-N-((S)-1,1-diethoxypropan-2-yl)-N-(quinolin-8-ylmethyl)propanamideHCID 67075208—
Reactant(S)-2-(1-allyl-2-(1-phenylethylcarbamoyl)hydrazinyl)acetic acidHCID 67075541—
Product2-allyl-2-(2-((S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1-oxopropan-2-ylamino)-2-oxoethyl)-N-((S)-1-phenylethyl)hydrazinecarboxamideHCID 6707568081.5%

Reaction Steps

According to the procedure described in the synthesis method of Compound II-1, (S)-2-(1-allyl-2-(1-phenylethylcarbamoyl)hydrazinyl)acetic acid (Compound VI-5) 133 mg (0.48 mmol) was coupled with (S)-2-amino-3-(4-tert-butoxyphenyl)-N—((S)-1,1-diethoxy-propan-2-yl)-N-(quinolin-8-ylmethyl)propanamide (Compound IV-3) 203 mg (0.4 mmol) and purified on silica gel column chromatography (chloroform:methanol=100:0 to 95:5) to obtain the title compound 250 mg (81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193734B2
Source datasetuspto-grants-2015_11
ORD IDord-d873517275c043dabede6042873d0344
Source noteuspto-grants-2015_11