HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → [4-({[4-(2-Tert-butylphenyl)piperazin-1-yl]carbonyl}amino)phenoxy]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl [4-({[4-(2-tert-butylphenyl)piperazin-1-yl]carbonyl}amino)phenoxy]acetate | HCID 66751108 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [4-({[4-(2-Tert-butylphenyl)piperazin-1-yl]carbonyl}amino)phenoxy]acetic acid | HCID 66792782 | 98.2% |
Reaction Steps
To an ice-cold stirred solution of methyl [4-({[4-(2-tert-butylphenyl)piperazin-1-yl]carbonyl}amino)phenoxy]acetate (Example 175, 0.240 g, 0.564 mmol) in THF (5 mL) was added 1 M lithium hydroxide solution (5 mL, 5 mmol). After 1 h the reaction mixture was acidified with 1 M HCl solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to provide [4-({[4-(2-tert-butylphenyl)piperazin-1-yl]carbonyl}amino)phenoxy]acetic acid (0.228 g, 98%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-f50883a9dc9b44299a341cf632262d48 |
| Source note | uspto-grants-2014_10 |