HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 14819159, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | HCID 14819133 | HCID 14819133 | — |
| Reactant | HCID 14819287 | HCID 14819287 | — |
| Product | HCID 14819159 | HCID 14819159 | — |
Reaction Steps
Conducting a reaction and treatments in the same manner as in Step (3) of Example 1 except that N-(2-oxo-3-tetrahydrofuranyl)-L-alanine hydrochloride was used in a form neutralized with N-methylmorpholine in place of Isomer BCD of N-(2-oxo-5-octyl-3-tetrahydrofuranyl)-L-alanine, was obtained as a colorless syrupy substance N-(2-oxo-3-tetrahydrofuranyl)-L-alanyl-L-proline benzyl ester [in the formula (I), R1 =R2 =H, R3 =CH3, R4 and R5 =--(CH2)3 --, R6 =-CH2Ph (Compound 13)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04876359 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-746122d82b1e4960b038b057c5e729f2 |
| Source note | uspto-grants-1989_10 |