HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphoric Acid → N-(6-methylthioquinolin-5-yl)-2-bromodecanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Bromodecanoic acid | HCID 98310 | — |
| Reactant | 5-Amino-6-methylthioquinoline | HCID 10397660 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(6-methylthioquinolin-5-yl)-2-bromodecanamide | HCID 19027925 | 62.1% |
Reaction Steps
To a stirred solution of 2-bromodecanoic acid (184 mg, 0.73 mmol) in CH2C12 (3.0 ml) was injected by syringe oxalyl chloride (0.06 ml, 105 mol %) and then DMF (1 drop). After stirring at room temperature for 1 hour, N-methyl morpoline (0.24 ml, 300 mol %) was added. To this mixture was injected a solution of 5-amino-6-methylthioquinoline (139 mg, 100 mol %) in CH2Cl2 (2.0 ml). After stirring at room temperature for an additional 30 min. the reaction mixture was diluted with CH2Cl2 (30 ml), poured over 1.0M H3PO4 (100 ml), and extracted with CH2Cl2 (3×30 ml). The combined extracts were dried (Na2SO4), evaporated, and chromatographed using 1% triethylamine:ethyl acetate as eluants to give the title compound (192 mg, 62% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05656634 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-5faf4540dabc4edf95c76e26bea1716b |
| Source note | uspto-grants-1997_08 |