HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178434Generated: October 31, 2026
Stannous chloride dihydrate → 4-((2-Amino-4-(quinolin-2-ylmethoxy)phenylamino)methyl)benzonitrile
https://huagongshe.com/reaction/2178434
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-((2-Nitro-4-(quinolin-2-ylmethoxy)phenylamino)methyl)benzonitrile | HCID 90414108 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-((2-Amino-4-(quinolin-2-ylmethoxy)phenylamino)methyl)benzonitrile | HCID 90414374 | — |
Reaction Steps
To a solution of 2-((4-fluoro-3-nitrophenoxy)methyl)quinoline (298 mg, 1 mmol) and 4-(aminomethyl)benzonitrile (132 mg, 1 mmol) in acetonitrile (1 mL) was added DIPEA (2 mL, 12 mmol). The mixture was stirred at 80° C. overnight. The mixture was cooled to RT, water (20 mL) was added, and the mixture was extracted with DCM (3×20 mL). The organics were combined, washed with brine (20 mL), dried (Na2SO4), filtered and concentrated to dryness. The residue was recrystallized from ethanol to give 4-((2-nitro-4-(quinolin-2-ylmethoxy)phenylamino)methyl)benzonitrile. The recrystallized 4-((2-nitro-4-(quinolin-2-ylmethoxy)phenylamino)methyl)benzonitrile (307 mg, 0.75 mmol) was then dissolved in ethanol (20 mL) and SnCl2.2H2O (1 g, 4.5 mmol) was added. The resulting mixture was stirred at 90° C. overnight. The mixture was cooled to RT and the pH adjusted to ˜pH 8-9 by the addition of sat. aq. NaHCO3. The aqueous mixture was stirred at RT for 30 min. and then extracted with DCM (3×20 mL). The organics were combined, washed with brine (20 mL), dried (Na2SO4), filtered and concentrated to dryness to afford the title compound, which was used without further purification. MS (ESI): mass calcd. for C24H20N4O, 380.16; m/z found, 381.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067917B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-c26a5b18ba7d4f4898320fdf645574bf |
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| Source note | uspto-grants-2015_06 |
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