HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-[[4-Bromo-1-[2-(4-fluorophenoxy)ethoxy]-2-naphthalenyl]carbonyl]-2-methylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 68841391 | HCID 68841391 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-[[4-Bromo-1-[2-(4-fluorophenoxy)ethoxy]-2-naphthalenyl]carbonyl]-2-methylalanine | HCID 24769566 | — |
Reaction Steps
61 mg 2-({4-bromo-1-[2-(4-fluoro-phenoxy)-ethoxy]-naphthalene-2-carbonyl}-amino)-2-methyl-propionic acid methyl ester in 0.5 ml THF, 0.36 ml of 2 M sodium hydroxide and 1.7 ml methanol were reacted in a microwave at 120° C. for 6 min. The reaction was then acidified with 2 M hydrochloric acid and extracted with ethyl acetate twice. The combined organic layers were dried over magnesium sulphate, and concentrated. After purification of the residue by RP-HPLC 27 mg of 2-({4-bromo-1-[2-(4-fluoro-phenoxy)-ethoxy]-naphthalene-2-carbonyl}-amino)-2-methyl-propionic acid were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501981B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-2cc396ab89324918b6e3f7ad630b51e9 |
| Source note | uspto-grants-2013_08 |