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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975585Generated: October 26, 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/975585

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 numberUS05608072
Source datasetuspto-grants-1997_03
ORD IDord-1ebf50a6f45e431f978f0f679b31e4c9
Source noteuspto-grants-1997_03