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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013089Generated: October 30, 2026

Potassium Cyanide → HCID 44243001, compound

https://huagongshe.com/reaction/1013089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 57908080HCID 57908080—
SolventMethanolHCID 887—
ProductHCID 44243001HCID 4424300179%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981904B2
Source datasetuspto-grants-2011_07
ORD IDord-0467708ed53148819fe1e8b03061f9b5
Source noteuspto-grants-2011_07