HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-isopropyloxazol-4-yl)-N-methylmethanamine → N-((N-Methyl-N-((2-isopropyl-4-oxazolyl)methyl)amino)carbonyl)-L-alanine Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-isopropyloxazol-4-yl)-N-methylmethanamine | HCID 10820784 | — |
| Reactant | Methyl N-[(4-nitrophenoxy)carbonyl]-L-valinate | HCID 15344176 | — |
| Reactant | N-(((4-nitrophenyl)oxy)carbonyl)-L-alanine methyl ester | HCID 54298210 | — |
| Product | N-((N-Methyl-N-((2-isopropyl-4-oxazolyl)methyl)amino)carbonyl)-L-alanine Methyl Ester | HCID 10708114 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05846987 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-2fd742d4ab3f44c2b90f1a05b248828b |
| Source note | uspto-grants-1998_12 |