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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457144Generated: 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/1457144

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 1 S, 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) δ 1.32 (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 numberUS05846987
Source datasetuspto-grants-1998_12
ORD IDord-2fd742d4ab3f44c2b90f1a05b248828b
Source noteuspto-grants-1998_12