HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl L-phenylalaninate hydrochloride → N-benzyloxycarbonyl (beta-benzyl)-L-aspartyl-L-phenylalanine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl L-phenylalaninate hydrochloride | HCID 75736 | — |
| Reactant | N-benzyloxycarbonyl-(beta-benzyl)-D,L-aspartic acid | HCID 18324139 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-benzyloxycarbonyl (beta-benzyl)-L-aspartyl-L-phenylalanine methyl ester | HCID 14876780 | 21.2% |
Reaction Steps
The process of Example 50 was repeated except that 715 mg (2.00 mmol) of N-benzyloxycarbonyl-(β-benzyl)-D,L-aspartic acid and 215 mg of L-phenylalanine methyl ester hydrochloride, 200 mg of Prolisin and 200 mg of the inhibitor were reacted. As a result, an 110 mg amount (yield of 21.2%) of N-benzyloxycarbonyl-(β-benzyl)-L-aspartyl-L-phenylalanine methyl ester having an [α]D22 = -12.8 (C-1.0 dimethylformamide) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04116768 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-a06e61057c8743539117e1cad29c7917 |
| Source note | uspto-grants-1978_09 |