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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52729Generated: October 25, 2026

1-(2-isopropyloxazol-4-yl)-N-methylmethanamine → N-((N-Methyl-N-((2-isopropyl-4-oxazolyl)methyl)amino)carbonyl)-L-alanine Methyl Ester

https://huagongshe.com/reaction/52729

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-isopropyloxazol-4-yl)-N-methylmethanamineHCID 10820784—
ReactantMethyl N-[(4-nitrophenoxy)carbonyl]-L-valinateHCID 15344176—
ReactantN-(((4-nitrophenyl)oxy)carbonyl)-L-alanine methyl esterHCID 54298210—
ProductN-((N-Methyl-N-((2-isopropyl-4-oxazolyl)methyl)amino)carbonyl)-L-alanine Methyl EsterHCID 1070811466%

Reaction Steps

Using the procedure of Example 1S, but replacing 2-isopropyl-4-(((N-methyl)amino)methyl)thiazole with 2-isopropyl-4-(((N-methyl)amino)methyl)-oxazole and relacing N-(((4-nitrophenyl)oxy)carbonyl)-L-valine methyl ester with N-(((4-nitrophenyl)oxy)carbonyl)-L-alanine methyl ester provided the desired compound in 66% yield. 1H NMR (CDCl3) δ1.32 (d, 6H), 1.42 (d, 3H), 2.96 (s, 3H), 3.05 (m, 1H), 3.75 (s, 3H), 4.30 (s, 2H), 4.47 (m, 1H), 5.80 (br d, 1H), 7.46 (s, 1H). Mass spectrum: (M+H)+ =284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616720
Source datasetuspto-grants-1997_04
ORD IDord-636ca2154b8340fd87a2cf1b2626271e
Source noteuspto-grants-1997_04