HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → HCID 44243001, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 57908080 | HCID 57908080 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 44243001 | HCID 44243001 | 79% |
Reaction Steps
A solution of 6B (1.0 equivalent) in MeOH (0.06M), was slowly added NH4Cl (1.2 equivalents) and 30% aq. NH3OH (0.06M) and stirred at room temperature for 30 minutes. The mixture was cooled at 0° C., and KCN was added in portions. After 12 hrs, 80% of MeOH was removed under reduced pressure, and then replaced MeOH with diethyl ether at 0° C. Filtered crystallized solid and washed crystals with cold diethyl ether twice to afford the 1-(3-(4-amino-4-cyanopiperidine-1-carbonyl)benzo[b]thiophen-2-yl)-3-ethylurea (6, 79%). Two rotamers observed (ratio 1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981904B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-0467708ed53148819fe1e8b03061f9b5 |
| Source note | uspto-grants-2011_07 |