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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612319Generated: October 26, 2026

2-(((Tert-butoxy)carbonyl)amino)butanoic acid → methyl N-{2-[(tert-butoxycarbonyl)amino]butanoyl}alaninate

https://huagongshe.com/reaction/1612319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(((Tert-butoxy)carbonyl)amino)butanoic acidHCID 333522—
ReactantMethyl 2-aminobutanoate hydrochlorideHCID 13283515—
Reactantmethyl{[N-(tert-butoxycarbonyl)-L-alanyl]amino}(cyclopropyl)acetateHCID 58583288—
Productmethyl N-{2-[(tert-butoxycarbonyl)amino]butanoyl}alaninateHCID 86588879—

Reaction Steps

Following the procedure for the preparation of methyl {[N-(tert-butoxycarbonyl)-L-alanyl]amino}(cyclopropyl)acetate but substituting N-Boc-alpha-aminobutyric acid and methyl 2-aminobutanoate hydrochloride and making non-critical variations provided the title compound as a solid: 1H NMR (CDCl3) δ 0.82-0.91, 1.24-1.38, 1.52, 1.68-2.05, 3.75, 4.20, 4.52-4.59, 5.05, 6.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06992087B2
Source datasetuspto-grants-2006_01
ORD IDord-643426b83b8640e6a0b606db6d9fbba1
Source noteuspto-grants-2006_01