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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603596Generated: November 1, 2026

tert-butyl N-(4-aminobutyl)carbamate → HCID 54175609, compound

https://huagongshe.com/reaction/1603596

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
Reactant4-[(2,6-Dibromo-4-pyridinyl)sulfonyl]anilineHCID 11014674—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54175609HCID 5417560977%

Reaction Conditions

Temperature60 °C

Reaction Steps

0.39 g (0.001 mol) of 4-(2,6-dibromopyridine-4-sulphonyl)-phenylamine was dissolved in 10 ml of dioxane and treated with 1.9 ml (0.01 mol) of N-tert.-butoxycarbonyl-1,4-diaminobutane. The mixture was stirred at 60° C. for 18 hrs., the solvent was removed and the residue was chromatographed on silica gel with ethyl acetate/hexane 1:1. There was obtained 0.36 g (77%) of tert-butyl [4-[4-(4-aminobenzenesulphonyl)-6-bromopyridin-2-ylamino]-butyl]-carbamate as a pale yellow oil. MS (ISP): me/e=501, 499 (C20H26BrN4O4S+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-1c81f32f3ec54f10a8ad69290fba298a
Source noteuspto-grants-1999_11