HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 178512943, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178512835 | HCID 178512835 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178512943 | HCID 178512943 | — |
Reaction Steps
From compound 8, in a manner similar to the synthesis of compound 2 (except that instead of trifluoroacetic acid use is made of its mixture with methylene chloride in the volume ratio of (1:1) α-benzyloxycarbonyl, ε-(nitroarginyl)lysylnitroarginylproline trifluoroacetate (compound 9) is obtained. The yield is 96%. αD20 =-12.0° (c=1, dimethylformamide). Ehis =0.52 (1 N acetic acid), Rf ==0.16 (B), 0.52 (C), 0.54 (D).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04285857 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-dab50a0612174c7ba5af033843c64a19 |
| Source note | uspto-grants-1981_08 |