HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22054562, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 22054485 | HCID 22054485 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 22054562 | HCID 22054562 | 65% |
Reaction Steps
Sodium triacetoxyborohydride (74 mg, 0.34 mmol) was added to a solution of 4-chloro-2-methyl-quinoline-7-carbaldehyde (example 13a, 50 mg, 0.24 mmol), 4-aminobenzonitrile (29 mg, 0.24 mmol), and acetic acid (88 mg, 1.5 mmol) in 1,2-dichloroethane (0.5 mL), then after 16 h the reaction mixture was partitioned between ethyl acetate and 2 M aq. sodium hydroxide solution. The organic layer was washed with brine, dried (MgSO4), and evaporated. Flash chromatography (SiO2, hexane/ethyl acetate 1:1) afforded the title compound (48 mg, 64%); White solid, ISP-MS: m/e=308.2 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07012073B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-ca115b81531b494a822a4dae5396fec9 |
| Source note | uspto-grants-2006_03 |