HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → HCID 86756745, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 86756747 | HCID 86756747 | — |
| Product | HCID 86756745 | HCID 86756745 | — |
Reaction Steps
In a manner analogous to that described in the first paragraph of Example 2, but using methanesulphonic acid in place of p-toluenesulphonic acid, starting from 0.2 g of (E)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-(methanesulphonyl)-4-methyl-2′-[(3-pyridyl)methyl]valerohydrazide there was obtained 0.177 g of (E)-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-2′-(methanesulphonyl)-4-methyl-2′-[(3-pyridyl)methyl]valerohydrazide methanesulphonate in the form of an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235787B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-9320e3871aa344879a6fe01d14877fb3 |
| Source note | uspto-grants-2001_05 |