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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616720 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-636ca2154b8340fd87a2cf1b2626271e |
| Source note | uspto-grants-1997_04 |