HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → Dicyclohexylcarbodiimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | HCID 19031950 | HCID 19031950 | — |
| Reactant | HCID 86748949 | HCID 86748949 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Product | Dicyclohexylcarbodiimide | HCID 10868 | — |
Reaction Steps
In a manner analogous to that described in Example from 295 mg of N2 -[3(S) [[L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide, 204 mg of 6-(benzyloxycarbonyl ) -2-naphthoic acid, 20 mg of hydroxybenzotriazole, 77 mg of N-ethylmorpholine and 151 mgof dicyclohexylcarbodiimide there were obtained, after chromatography on silica gel using System G for the elution, 340 mg of N2 -[3(S)-[[N-[6-(benzyloxycarbonyl)-2-naphthoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide as an off-white solid from ethyl acetate/n-hexane: MS: m/e 736 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446161 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-c0a43f9595c34f8bbce7700641989664 |
| Source note | uspto-grants-1995_08 |