HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86598325, compound → HCID 69320224, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86598325 | HCID 86598325 | — |
| Reactant | HCID 86598326 | HCID 86598326 | — |
| Product | HCID 69320224 | HCID 69320224 | — |
Reaction Steps
In a similar manner to Example 49-1), 3-[4-(4-hydroxyphenoxy)-phenoxy]-L-phenylalanine was synthesized by deprotecting by a conventional method from N-trifluoroacetyl-3-(4-hydroxyphenoxy)-L-phenylalanine ethyl ester via N-trifluoroacetyl-3-[4-(4-methoxyphenoxy)phenoxy]-L-phenylalanine ethyl ester. N-Trifluoroacetyl-3-[4-(4-methoxyphenoxy)phenoxy]-L-phenylalanine ethyl ester: m.p.: 67-71° C.; IR (Nujol): 3324, 1745, 1707, 1559, 1507, 1501 cm−1; APCI-MS m/z: 504 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07345068B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-44db2a5aa00741b38bc00d51c3f0bfcc |
| Source note | uspto-grants-2008_03 |