HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252922Generated: October 26, 2026
Hydrazine → 2-Hydrazinyl-5,6,7,8,9,10-hexahydrocyclooct[b]pyridine
https://huagongshe.com/reaction/252922
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-Chloro-5,6,7,8,9,10-hexahydrocycloocta[b]pyridine | HCID 58199532 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Hydrazinyl-5,6,7,8,9,10-hexahydrocyclooct[b]pyridine | HCID 55281928 | — |
Reaction Steps
2-Chloro-5,6,7,8,9,10-hexahydrocycloocta[b]pyridine was treated with ethanol (20 mL) and anhydrous hydrazine (5 mL) in a sealed tube at 150° C. bath temperature for 7 h. Initial experiments showed that the addition did not proceed in boiling ethanol at atmospheric pressure. HPLC showed that the addition was incomplete, so the reaction mixture was heated at 150° C. for a further 7 h. The solvent was removed under reduced pressure and the residue was purified by flash chromatography on silica gel, eluting with 95% dichloromethane and 5% of a 2M solution of ammonia in methanol; 1H NMR (CDCl3, 300 MHz) 7.19 (d, 1H), 6.51 (d, 1H), 5.85 (br s, 1H), 3.77 (br s, 2H), 2.79 (m, 2H), 2.63 (m, 2H), 1.73 (m, 2H), 1.62 (m, 2H), 1.36 (m, 4H) ppm; 13C NMR (CDCl3, 75 MHz) 156.87, 158.54, 138.81, 126.67, 104.58, 34.72, 32.67, 31.45, 30.85, 26.41, 26.37;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872000B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-be8f102f275944f0ba90750c7ed42592 |
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| Source note | uspto-grants-2011_01 |
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