HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 86756034, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 86756035 | HCID 86756035 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86756034 | HCID 86756034 | 102.1% |
Reaction Steps
To a pre-dried flask under nitrogen atmosphere was added cis-8-amino-4-[(3,5-bis-trifluoromethyl-benzyl)-methoxycarbonyl-amino]-6-chloro-2-methyl-3,4-dihydro-2H-quinoline-1-carboxylic acid ethyl ester (Example 109) (30 mg, 0.053 mmol), followed by anhydrous dichloromethane (2 mL), pyridine (0.5 mL), and acetyl chloride (0.015 mL, 0.21 mmol). The reaction was stirred overnight at room temperature before ethyl acetate was added, and the mixture was extracted three times with 1N HCl, followed by brine. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to give the title product (33 mg, 100%) MS m/z 610 (M++H); 1H NMR (CDCl3) δ 7.8 (bs, 2H), 7.7 (bs, 1H), 7.65 (bs, 1H), 6.8 (bs, 1H), 3.8 (s, 3H), 2.1 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06395751B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-44437af715a44ed084fc416d3810d6be |
| Source note | uspto-grants-2002_05 |