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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415626Generated: November 2, 2026

Water → N-{4-((7-chloroquinolin-4-yl)amino)cyclohexyl}thiourea

https://huagongshe.com/reaction/2415626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium thiocyanateHCID 15666—
ReactantHCID 178477879HCID 178477879—
SolventAcetoneHCID 180—
ProductN-{4-((7-chloroquinolin-4-yl)amino)cyclohexyl}thioureaHCID 2264182447%

Reaction Steps

Ammonium thiocyanate (320 mg, 4.2 mmol) was dissolved in 85 mL dry acetone. A solution of benzoyl chloride (590 mg, 4.2 mmol) in 10 mL dry acetone was added dropwise and heated at reflux for 30 minutes. A solution of 23A cis-N,N′-bis(7-chloroquinolin-4-yl)cyclohexane-1,4-diamine (1 g, 3.6 mmol) in 10 mL dry acetone was added dropwise to the refluxing solution. After the addition, the solution was poured into 100 mL of water. The resulting solid was filtered and heated in 30 mL of 10% sodium hydroxide until dissolved. The solution was then allowed to cool and was placed in the freezer overnight. The white solid was filtered and dried under vacumn to give 565 mg, 47% yield. MS ESI(+)Q1MS m/z 334 (M+H)+; 1 H NMR (300 MHz, DMSO) δ ppm 8.38-8.42 (m, 2 H), 8.78 (d, 1 H), 7.44 (dd, 1 H), 6.66-6.69 (m, 2 H), 6.53 (d, 1 H), 4.17 (m, 1 H), 3.61 (m, 1 H), 1.96-2.06 (m, 4H), 1.65-1.84 (m, 8 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818772B2
Source datasetuspto-grants-2004_11
ORD IDord-6b97aaae65f549c4a473c0d6f53209fc
Source noteuspto-grants-2004_11