HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Piperidin-4-ylidenehydroxylamine → HCID 178511976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Piperidin-4-ylidenehydroxylamine | HCID 12849639 | — |
| Reactant | 2-Biphenylylcyanamide | HCID 19089221 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178511976 | HCID 178511976 | — |
Reaction Steps
A mixture of 2-biphenylylcyanamide (3.9 g), 4-piperidone oxime (4.5 g) and ethanol (50 ml) was stirred at ambient temperature for 6 hours and then at 50°-60° C. for 5 hours to give a brown solid which was purified by chromatography on an aluminia column eluted successively with hexane, 1:4, 2:3, 3:2 and 4:1 mixtures of dichloromethane and hexane and the 99:1 mixture of dichloromethane and methanol to yield a solid which was recrystallised from ethyl acetate to give N-(2-biphenylyl)-4-hydroxyiminopiperidine-1-carboxamidine (m.p. 175°-176° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05302720 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-465a9d0715a04f54ba8dd0c1e2445d0f |
| Source note | uspto-grants-1994_04 |