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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517513Generated: October 29, 2026

Tert-butyl(4-chloro-but-2-ynyloxy)-dimethylsilane → methyl (S)-3-{4-[4-(tert-butyldimethylsilanyloxy)but-2-ynyloxy]benzoyl-amino}-2-(4-methanesulphonylpiperazin-1-yl)propanoate

https://huagongshe.com/reaction/517513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl(4-chloro-but-2-ynyloxy)-dimethylsilaneHCID 13403316—
Reactantmethyl (S)-3-(4-hydroxybenzoylamino)-2-(4-methanesulphonylpiperazin-1-yl)propanoateHCID 67056914—
Productmethyl (S)-3-{4-[4-(tert-butyldimethylsilanyloxy)but-2-ynyloxy]benzoyl-amino}-2-(4-methanesulphonylpiperazin-1-yl)propanoateHCID 8666791089.8%

Reaction Steps

In a manner similar to example 4-5, starting from 400 mg (1 mmol) of methyl (S)-3-(4-hydroxybenzoylamino)-2-(4-methanesulphonylpiperazin-1-yl)propanoate (prepared as described in example 4-4) and from 270 mg (1.2 mmol) of tert-butyl(4-chloro-but-2-ynyloxy)-dimethylsilane; 510 mg (88%) of methyl (S)-3-{4-[4-(tert-butyldimethylsilanyloxy)but-2-ynyloxy]benzoyl-amino}-2-(4-methanesulphonylpiperazin-1-yl)propanoate are obtained in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115102B2
Source datasetuspto-grants-2015_08
ORD IDord-d30af802f3ff49ddb1798a0ed7bd41f8
Source noteuspto-grants-2015_08