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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824237Generated: October 31, 2026

methyl N-{2-[(tert-butoxycarbonyl)amino]butanoyl}alaninate → methyl N-(2-aminobutanoyl)alaninate hydrochloride

https://huagongshe.com/reaction/1824237

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl N-{2-[(tert-butoxycarbonyl)amino]butanoyl}alaninateHCID 86588879—
Reactantmethyl(L-alanylamino)(cyclopropyl)acetate hydrochlorideHCID 86588880—
Productmethyl N-(2-aminobutanoyl)alaninate hydrochlorideHCID 86588882—

Reaction Steps

Following the procedure for the preparation of methyl(L-alanylamino)(cyclopropyl)acetate hydrochloride but substituting methyl N-{2-[(tert-butoxycarbonyl)amino]butanoyl}alaninate and making non-critical variations provided the title compound asia solid: 1H NMR (DMSO-d6) δ 0.86–0.92, 1.39–1.41, 1.62–1.82, 3.64, 3.92, 4.18–4.23, 8.36, 8.92.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041672B2
Source datasetuspto-grants-2006_05
ORD IDord-7508a023a2964348aff876be1ea4456b
Source noteuspto-grants-2006_05