HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 57500393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | HCID 57500374 | HCID 57500374 | — |
| Product | HCID 57500393 | HCID 57500393 | — |
Reaction Steps
By following the process described in stage G of Example 42, the coupling of benzyl 5-[(1-{[3-(2-aminoethoxy)benzoyl]amino}-2-methylindolizin-3-yl)carbonyl]-2-[(trifluoroacetyl)amino]benzoate (described in stage F, Example 42) with N-tert-butoxycarbonylglycine is carried out. The compound obtained is then deprotected with trifluoroacetic acid to give the amine according to the process described in stage F of Example 42.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120819B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-ae1b9327c5e94d3baa0761b21c12fd3a |
| Source note | uspto-grants-2015_09 |