HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyloxycarbonylglycine → HCID 20163754, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | HCID 20163722 | HCID 20163722 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 20163754 | HCID 20163754 | — |
Reaction Steps
The same procedure of the example 2, starting from N-benzyloxycarbonylglycine and 2-isopropyl-5-methyl-4-imidazolidinone afforded 1-(2-benzyloxycarbonylaminoacetyl)-2-isopropyl-5-methyl-4-imidazolidinone as a diastereoisomeric mixture Rf=0.52 and 0.57 (dichloromethane/methanol 9:1, silica gel plates) then the oily title compound as a diastereoisomeric mixture, Rf=0.24 and 0.27 (dichloromethane/methanol 7:3, silica gel plates). Mass spectrum (E.I., 70 e V, 1.5 mA), m/z=156 (M.+ --C3H7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04703054 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-fd0893dc1a5a4a95a0eb6962ae370566 |
| Source note | uspto-grants-1987_10 |