HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707344Generated: October 30, 2026
Acetic Acid → N2-(1-(quinolin-2-yl)azetidin-3-yl)pyridine-2,3-diamine
https://huagongshe.com/reaction/707344
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-nitro-N-(1-(quinolin-2-yl)azetidin-3-yl)pyridin-2-amine | HCID 86694202 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N2-(1-(quinolin-2-yl)azetidin-3-yl)pyridine-2,3-diamine | HCID 86694203 | 81.2% |
Reaction Steps
To a solution of 3-nitro-N-(1-(quinolin-2-yl)azetidin-3-yl)pyridin-2-amine (1.05 g, 3.20 mmol) in ethanol (30 mL) and water (10 mL) was added iron (448 mg, 8.0 mmol) and acetic acid (240 mg, 4.0 mmol) slowly dropwise. The mixture was heated at 95° C. until TLC analysis confirmed the absence of starting materials. The reaction mixture was filtered through a plug of CELITE™ washing with methanol. The black filtrate was concentrated in vacuo, treated with brine (40 mL) and extracted with dichloromethane (3×60 mL). The combined organic extracts were washed with water (30 mL) and brine (30 mL) and then dried over sodium sulfate. The filtrate was evaporated in vacuo to give N2-(1-(quinolin-2-yl)azetidin-3-yl)pyridine-2,3-diamine (0.744 g, 2.6 mmol, yield 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174992B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-b28e388cbf574c348ff6dcbf723cd7b0 |
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| Source note | uspto-grants-2015_11 |
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