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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773616Generated: November 2, 2026

1,2-Diaminocyclohexane, cis- → HCID 56646341, compound

https://huagongshe.com/reaction/1773616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Diaminocyclohexane, cis-HCID 342917—
ReactantHCID 66664866HCID 66664866—
ReactantHCID 86661376HCID 86661376—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 56646341HCID 56646341—

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of the mixture of 80 mg of 2-Chloro-thieno[3,2-d]pyrimidine-7-carboxylic acid benzo[1,3]dioxol-5-ylamide and 2-(Benzotriazol-1-yloxy)-thieno[3,2-d]pyrimidine-7-carboxylic acid benzo[1,3]dioxol-5-ylamide (from step a) and 0.17 g (1.41 mmole) of cis-1,2-diaminocyclohexane in Dioxane (3 mL) was stirred at 60° C. for overnight. The reaction were cooled down and diluted with CH2Cl2, washed with aqueous Na2CO3, brine, dried over anhydrous Na2SO4, concentrated and purified by flash chromatography (silica gel, 40 g, 0% to 30% MeOH (0.7 N) in CH2Cl2) to 40 mg of 2-(cis-2-Amino-cyclohexylamino)-thieno[3,2-d]pyrimidine-7-carboxylic acid benzo[1,3]dioxol-5-ylamide as light yellow solid. MH+/Z=412.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255110B2
Source datasetuspto-grants-2016_02
ORD IDord-fbb3b9215f804c0f8d51aec260dc161b
Source noteuspto-grants-2016_02