HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylpentanehydrazide → HCID 86756924, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylpentanehydrazide | HCID 22994823 | — |
| Reactant | HCID 86756925 | HCID 86756925 | — |
| Reactant | HCID 86756927 | HCID 86756927 | — |
| Product | HCID 86756924 | HCID 86756924 | — |
Reaction Steps
In a manner analogous to that described in the first paragraph of Example 5, starting from 0.058 g of a mixture of (E)-2′-(D-alanyl)-2′-cyclopentyl-2(R)-[1(S)-[tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-4-methylvalero-hydrazide and (E)-2′-(D-alanyl)-2′-cyclopentyl-2(S)-[1(R)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-4-methylvalerohydrazide there was obtained 0.048 mg of a mixture of (E)-2′-(D-alanyl)-2′-cyclopentyl-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-4-methylvalerohydrazide p-toluene-sulphonate and (E)-2′-(D-alanyl)-2′-cyclopentyl-2(S)-[1(R)-(hydroxycarbonyl)-4-phenyl-3-butenyl]-methylvalerohydrazide p-toluenesulphonate in the form of a pale pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06239151B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-7f81fb98bf594095abe58ee7ff1281e6 |
| Source note | uspto-grants-2001_05 |