HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430074Generated: October 26, 2026
Hydrochloric Acid → HCID 18353676, compound
https://huagongshe.com/reaction/430074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-[3,3-Diethoxypropylamino]-4-methoxyquinoline | HCID 18353658 | — |
| Reactant | HCID 18353681 | HCID 18353681 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18353676 | HCID 18353676 | 80.9% |
Reaction Steps
2-[3,3-Diethoxypropylamino]-4-methoxyquinoline (0.046 g, 0.15 mmol) in THF (4 ml) was treated with 0.5M HCl (2 ml) for 10 min. The reaction mixture was evaporated to dryness and to the residue in methanol/HOAc (1 ml/0.018 ml) was added NaOAc (0.024 g, 0.3 mmol), 2-(3,4-dichlorophenyl)azetidine (0.03 g) and sodium cyanoborohydride (0.009 g, 0.15 mmol). After reaction for 40 min at 20° C., the reaction was evaporated to dryness under reduced pressure, and the residue partitioned between ethyl acetate and sat. sodium bicarbonate. The organic layer was dried, evaporated to dryness under reduced pressure and purified by chromatography on silica gel eluting with 1-3% (9:1 MeOH/NH3) in dichloromethane to give the title compound as a colourless gum (50 mg, 80%); δH (CD3OD) 1.55 (2H, m), 2.0 (1H, m), 2.25 (1H, m), 2.45-2.7 (2H, m), 2.8 (1H, m), 3.2-3.4 (4H, m), 3.9 (3H, s), 3.95 (1H, t), 6.0 (1H, s), 7.05 (1H, t), 7.15-7.5 (5H, m), 7.8 (1H, d); MS (ES+) 416/418 (47/32%, MH+), 244 (50), 201 (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06320051B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-a3078d8c9b1840909e6517502c166810 |
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| Source note | uspto-grants-2001_11 |
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