HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 4-{4-[3-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | HCID 58494034 | HCID 58494034 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-{4-[3-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}butanoic acid | HCID 54579597 | 48.1% |
Reaction Steps
To a solution of 4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]piperidine (D122) (108 mg, 0.244 mmol) and ethyl 4-bromobutanoate (95 mg, 0.489 mmol) in N,N-Dimethylformamide (DMF) (8 mL) was added K2CO3 (223 mg, 1.614 mmol). This solution was sealed and stirred for overnight at room temperature. To the above solution was added Isopropanol (10.00 mL) and Water (2 mL) and sodium hydroxide (0.5 mL, 3.05 mmol). The solution was sealed and stirred for 5 h at 40° C. The reaction was neutrolized by AcOH, dried and purified by Mass Directed AutoPrep to afford 4-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}butanoic acid (E102) (62 mg) as a TFA salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389508B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-fb6df607ebc447998544fdf1d3f6ee09 |
| Source note | uspto-grants-2013_03 |