HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Phenyl diethanolamine → (S)-3-(3-bromo-4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)phenyl)-2-(4-phenylpiperazin-1-yl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Phenyl diethanolamine | HCID 8416 | — |
| Reactant | (2S)-2-amino-3-{3-bromo-4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)-ethoxy]-phenyl}-propionic acid | HCID 69063835 | — |
| Product | (S)-3-(3-bromo-4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)phenyl)-2-(4-phenylpiperazin-1-yl)propanoic acid | HCID 11512673 | 30% |
Reaction Steps
Following the procedures described in Example 1, Intermediate 3B was used in place of Intermediate 3A, and 2,2′-(phenylazanediyl)diethanol was used in place of 2,2′-(m-tolylazanediyl)diethanol to give (2S)-3-{3-bromo-4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)-ethoxy]-phenyl}-2-(4-phenylpiperazin-1-yl)-propanoic acid as a white solid with the yield of 30% and mp of 220-222° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544687B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-57f2ce6011d64248899ef33cfec1f238 |
| Source note | uspto-grants-2009_06 |