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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254378Generated: October 30, 2026

{4-[4-(3-Carbamoylpropylamino)phenyl]butyl}carbamic acid tert-butyl ester → 4-[4-(4-Aminobutyl)phenylamino]butyramide

https://huagongshe.com/reaction/254378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{4-[4-(3-Carbamoylpropylamino)phenyl]butyl}carbamic acid tert-butyl esterHCID 58664823—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product4-[4-(4-Aminobutyl)phenylamino]butyramideHCID 58664835—

Reaction Steps

{4-[4-(3-Carbamoylpropylamino)phenyl]butyl}carbamic acid tert-butyl ester 430 (0.23 g, 0.66 mmol) was cooled to 0° C. in an ice bath. A cold solution of TFA/dichloromethane (10 mL) was added. The reaction was slowly warmed to room temperature and stirred for 30 minutes. The solvent was evaporated in vacuo to provide 440. 1H NMR (300 MHz, CD3OD) δ 1.69 (m, 4H), 1.95 (m, 2H), 2.47 (m, 2H), 2.71 (m, 2H), 2.93 (m, 2H), 3.39 (m, 2H), 7.39 (s, 4H). m/z (ESI) 250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875619B2
Source datasetuspto-grants-2011_01
ORD IDord-06f20629399a42e6b57a46d70182a8f2
Source noteuspto-grants-2011_01