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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415676Generated: November 2, 2026

tert-Butyl (piperazin-1-yl)acetate → HCID 53864541, compound

https://huagongshe.com/reaction/1415676

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (piperazin-1-yl)acetateHCID 2757326—
ReactantHCID 9821029HCID 9821029—
ReactantHCID 53812397HCID 53812397—
ReactantBenzyl [amino(methylsulfanyl)methylene]carbamateHCID 140362141—
ProductHCID 53864541HCID 53864541—

Reaction Steps

3-(3-(4-amidinopiperazin-1-ylacetamido)benzamido)propionic acid, m.p. 270° (decomposition), from benzyl 3-(3-(4-CBZ-amidinopiperazin-1-ylacetamido)benzamido)propionate (FAB 601; obtainable by reacting tert-butyl piperazin-1-ylacetate with N-CBZ-S-methylisothiourea to give tert-butyl 4-CBZ-amidinopiperazin-1-ylacetate, cleaving the tert-butyl group with 4 N HCl in dioxane and condensing the resulting 4-CBZ-amidinopiperazin-1-ylacetic acid with benzyl 3-(3-aminobenzamido)propionate);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908843
Source datasetuspto-grants-1999_06
ORD IDord-90bdff9b7c8a4264b06d3c5f7ba2c8b9
Source noteuspto-grants-1999_06