HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1R)-1-(2-chlorophenyl)ethan-1-ol → 5-(4-{4-[(1R)-1-(2-chlorophenyl)ethoxycarbonylamino]-3-isoxazolyl}phenyl)-4-pentenoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1R)-1-(2-chlorophenyl)ethan-1-ol | HCID 6999092 | — |
| Reactant | 3-(4-Iodophenyl)isoxazole-4-carboxylic acid | HCID 68880793 | — |
| Reactant | methyl 5-(4-{4-[(1R)-1-(2-chlorophenyl)ethoxycarbonylamino]-3-isoxazolyl}phenyl)-4-pentenoate | HCID 68881708 | — |
| Product | 5-(4-{4-[(1R)-1-(2-chlorophenyl)ethoxycarbonylamino]-3-isoxazolyl}phenyl)-4-pentenoic acid | HCID 68881703 | — |
Reaction Steps
According to methods similar to those of Step 5 and Step 6 of Example 19 using 3-(4-iodophenyl)isoxazole-4-carboxylic acid and (R)-2-chloro-α-methylbenzyl alcohol, methyl 5-(4-{4-[(1R)-1-(2-chlorophenyl)ethoxycarbonylamino]-3-isoxazolyl}phenyl)-4-pentenoate was synthesized, which was reacted in the same manner as in Example 2 to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517996B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-732bdbb24332403a902fc8b37d7f467f |
| Source note | uspto-grants-2009_04 |