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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718988Generated: October 31, 2026

2-(2-((4-Chlorobenzyl)carbamoyl)-1-methylhydrazinyl)acetic acid → (S)-tert-butyl 4-((benzo[b]thiophen-3-ylmethyl)((S)-1,1-diethoxypropan-2-yl)amino)-3-(2-(2-(4-chlorobenzylcarbamoyl)-1-methylhydrazinyl)acetamido)-4-oxobutanoate

https://huagongshe.com/reaction/718988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-((4-Chlorobenzyl)carbamoyl)-1-methylhydrazinyl)acetic acidHCID 53397501—
Reactant(S)-tert-butyl 3-amino-4-((benzo[b]thiophen-3-ylmethyl)((S)-1,1-diethoxypropan-2-yl)amino)-4-oxobutanoateHCID 67075220—
Product(S)-tert-butyl 4-((benzo[b]thiophen-3-ylmethyl)((S)-1,1-diethoxypropan-2-yl)amino)-3-(2-(2-(4-chlorobenzylcarbamoyl)-1-methylhydrazinyl)acetamido)-4-oxobutanoateHCID 67088509—

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) 88 mg (0.32 mmol) was coupled with (S)-tert-butyl 3-amino-4-((benzo[b]thiophen-3-ylmethyl)-((S)-1,1-diethoxypropan-2-yl)amino)-4-oxobutanoate (Compound IV-18) 100 mg (0.22 mmol) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193734B2
Source datasetuspto-grants-2015_11
ORD IDord-51c6f5b8e3d54f46a06444f569e3158f
Source noteuspto-grants-2015_11