HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → Dicyclohexylcarbodiimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 3-{[(Benzyloxy)carbonyl]amino}naphthalene-2-carboxylic acid | HCID 54463711 | — |
| 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 27, from 295 mg of N2 -[3(S)-[[L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide, 214 mg of 3-(benzyloxyformamido)-2-naphthoic acid, 90 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, 380 mg of N2 -[3(S)-[[N-[3-(benzyloxyformamido)-2-naphthoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide as a white solid from methanol: MS: m/e 751 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446161 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-cc380c5e5b9e491b97f7916f159f3ed5 |
| Source note | uspto-grants-1995_08 |