HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Amino-5-cyano-6-thien-3-ylpyridine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Reactant | Methyl 4-amino-5-cyano-6-ethoxypicolinate | HCID 40151899 | — |
| Solvent | Dimethyl ether water ethanol | HCID 86620092 | — |
| Product | 4-Amino-5-cyano-6-thien-3-ylpyridine-2-carboxylic acid | HCID 66920993 | 21% |
Reaction Steps
A suspension of Example 181D (212 mg, 1.0 mmol), 3-thiopheneboronic acid (134 mg, 1.05 mmol), dichlorobis(triphenylphosphine)-palladium(II) (Ph3P)2PdCl2 (7 mg, 0.01 mmol), and Na2CO3 (212 mg, 2.0 mmol) in dimethyl ether: water: ethanol (7:3:2, 4 mL) was heated at 150° C. for 10 minutes in a microwave reactor. The crude mixture was acidified with 2N HCl (2 mL) and partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, filtered and concentrated. It was triturated with acetonitrile to provide the titled compound (51 mg, 21% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888374B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-d450fab6edce4f47b164fbe5061a9ef6 |
| Source note | uspto-grants-2011_02 |