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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718964Generated: October 25, 2026

2-(2-((4-Chlorobenzyl)carbamoyl)-1-methylhydrazinyl)acetic acid → 4-(4-chlorobenzyl)-1-(2-((S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxy-propan-2-yl)(quinolin-8-ylmethyl)amino)-1-oxopropan-2-ylamino)-2-oxoethyl)-1-methylsemicarbazide

https://huagongshe.com/reaction/718964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-((4-Chlorobenzyl)carbamoyl)-1-methylhydrazinyl)acetic acidHCID 53397501—
Reactant(S)-2-amino-3-(4-tert-butoxyphenyl)-N-((S)-1,1-diethoxypropan-2-yl)-N-(quinolin-8-ylmethyl)propanamideHCID 67075208—
Product4-(4-chlorobenzyl)-1-(2-((S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxy-propan-2-yl)(quinolin-8-ylmethyl)amino)-1-oxopropan-2-ylamino)-2-oxoethyl)-1-methylsemicarbazideHCID 67075515—

Reaction Steps

According to the procedure described in the synthesis method of Compound II-15, 2-(2-(4-chlorobenzylcarbamoyl)-1-methylhydrazinyl)acetic acid (Compound VI-7) 80 mg (0.30 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) 100 mg (0.20 mmol) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193734B2
Source datasetuspto-grants-2015_11
ORD IDord-ef12c10079144beea7882fc1c3e83ebd
Source noteuspto-grants-2015_11