HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Oxobutanoic acid → HCID 66548249, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Oxobutanoic acid | HCID 1112 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 86712517 | HCID 86712517 | — |
| Product | HCID 66548249 | HCID 66548249 | — |
Reaction Steps
The title compound was synthesized by analogy with the synthesis process of Example 1 by reacting 45 mg (47 μmol) N-methyl-L-valyl-N-[(3R,4S,5S)-3-methoxy-1-{(2S)-2-[(1R,2R)-1-methoxy-3-{[(2S,3E)-4-[4-(methoxycarbonyl)phenyl]-1-phenylbut-3-en-2-yl}amino)-2-methyl-3-oxopropyl]pyrrolidin-1-yl}-5-methyl-1-oxoheptan-4-yl]-N-methyl-L-valinamide trifluoroacetic acid salt (intermediate 23) with a 15% aqueous solution of 4-oxobutanoic acid in the presence of sodium cyanoborohydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029406B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-46b049a2f6e04260be234775cbf7445f |
| Source note | uspto-grants-2015_05 |