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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986237Generated: October 30, 2026

1,4-Cyclohexanedimethanamine → HCID 178511242, compound

https://huagongshe.com/reaction/1986237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedimethanamineHCID 17354—
Reactant4-(1-Benzothiophen-2-yl)-2-chloropyrimidineHCID 14745025—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductHCID 178511242HCID 17851124288%

Reaction Steps

4-Aminomethyl-cyclohexylmethyl-amine (cis/trans-mixture, ca. 2:1) (1.28 g, 9.00 mmol) is added to a stirred suspension of 4-benzo[b]thiophen-2-yl-2-chloro-pyrimidine (986 mg, 4.00 mmol) in isopropanol (13 mL) at ambient temperature under nitrogen. The resultant mixture is heated at 110° C. for 20 hours. At ambient temperature the mixture is diluted with dichloromethane (40 mL), washed with 1N NaOH (13 mL), and dried (MgSO4). After concentration and subsequent chromatographic purification on silica gel, eluting with 2 M NH3/MeOH in dichloromethane 0-20%, the title compound is obtained as a 2:1 cis/trans-mixture (1.24 g, 88% yield). ES+(m/z) 353 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-a5316583bb2d43eaaa2f0bc851987d1a
Source noteuspto-grants-2009_06