It forms the core benzofuran scaffold of the drug and is coupled with the chiral piperidine moiety in subsequent steps. This coupling, followed by salt formation, leads to the final Prucalopride Succinate, ensuring the correct pharmacophore and activity of the prokinetic agent. 4‑Amino‑5‑chloro‑2,3‑dihydrobenzofuran‑7‑carboxylic acid is a key intermediate in the synthesis of Prucalopride Succinate.
4-Amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid
| API Name | Prucalopride succinate |
|---|---|
| CAS No | 123654-26-2 |
| Molecular Formula | C9H8ClNO3 |
| Molecular Weight | 213.62 g/mol |
| Synonyms | 4-amino-5-chloro-2,3-dihydro-1-benzofuran-7-carboxylic acid |
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Frequently Asked Questions
It forms the core benzofuran scaffold of the drug and is coupled with the chiral piperidine moiety in subsequent steps. This coupling, followed by salt formation, leads to the final Prucalopride Succinate, ensuring the correct pharmacophore and activity of the prokinetic agent. 4‑Amino‑5‑chloro‑2,3‑dihydrobenzofuran‑7‑carboxylic acid is a key intermediate in the synthesis of Prucalopride Succinate.
The CAS number of 4-Amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid is 123654-26-2.
The molecular formula of 4-Amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid is C9H8ClNO3.
The listed molecular weight of 4-Amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid is 213.62 g/mol.
4-Amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid is listed as being used in connection with the following API: Prucalopride succinate.
The listed synonym or IUPAC name for 4-Amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid is 4-amino-5-chloro-2,3-dihydro-1-benzofuran-7-carboxylic acid.