Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 9951833 | HCID 9951833 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70278872 | HCID 70278872 | 52% |
Reaction Steps
A solution of 4-(1-isopropyl-4,4,6-trimethyl-1,2,3,4-tetrahydroquinolin-7-ylamino)-benzoic acid ethyl ester (Compound 46, 64.4 mg, 0.1692 mmol), acetaldehyde (37.2 mg, 0.8462 mmol), sodium cyanoborohydride (53.2 mg, 0.8462 mmol), acetic acid (0.125 mL), and acetonitrile (1 mL) was stirred at room temperature overnight. The solvent was removed and the residue was purified by silica gel chromatography (10% ethyl acetate in hexane, Rf=0.44) to give the title compound (71.2 mg, 52%) as a solid: 1H NMR (300 MHz, CDCl3): δ1.15 (d, 6 H, J=6.5 Hz), 1.27 (t, 3 H, J=7.1 Hz), 1.31 (s, 6 H), 1.35 (t, 3 H, J=7.1 Hz), 1.74 (t, 2 H, J=6.0 Hz), 1.96 (s, 3 H), 3.15 (t, 2 H, J=6.0 Hz), 3.68 (d, 2 H, J=5.9), 3.98 (sp, 1 H, J=6.5 Hz), 4.31 (q, 2 H, J=7.1 Hz), 6.43 (s, 1 H), 6.49 (d, 2 H, J=8.9 Hz), 7.08 (s, 1 H), 7.84 (d, 2 H, J=8.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127382 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-46a81c1f878e445383ad0cb9cb4f9925 |
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| Source note | uspto-grants-2000_10 |
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