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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920675Generated: October 31, 2026

1-N,2-N-dimethylcyclohexane-1,2-diamine → HCID 86731168, compound

https://huagongshe.com/reaction/920675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
Reactant4-(4-Iodobenzyl)morpholineHCID 2795500—
ReactantHCID 86731169HCID 86731169—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86731168HCID 86731168100.4%

Reaction Conditions

Temperature195 °C

Reaction Steps

A solution of N-butyl-7-(4-((tert-butyldimethylsilyl)oxy)cyclohexyl)-5H-pyrrolo[3,2-d]pyrimidin-2-amine (59 mg, 0.14653 mmol) and 4-iodobenzyl morpholine (67 mg, 0.22 mmol) in NMP (1 mL) was added CuI (3 mg, 0.022 mmol) and N,N′-dimethylcyclohexane-1,2-diamine (2 mg, 0.044 mmol). The reaction mixture was stirred under microwave irradiation at 195° C. for 30 min. Then the reaction was diluted with EtOAc. The organic layer was dried (MgSO4), filtered and concentrated. The residue was purified by ISCO to provide the desired product (85 mg, 99%). 1H NMR (400 MHz, CDCl3) δ 8.48 (s, 1H), 7.36 (d, J=8 Hz, 2H), 7.25 (d, J=8 Hz, 2H), 7.17 (s, 1H), 4.86 (s, 1H), 3.71-3.52 (m, 4H), 3.44-3.38 (m, 4H), 3.32-3.17 (m, 1H), 2.81-2.71 (m, 2H), 2.45-2.33 (m, 4H), 2.15-2.04 (m, 2H), 1.96-1.83 (m, 2H), 1.61-1.29 (m, 8H), 0.94-0.75 (m, 12H), 0.00 (s, 6H). MS m/z 578.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273056B2
Source datasetuspto-grants-2016_03
ORD IDord-b5c9b00bbef540ff8fbda56cb39c9359
Source noteuspto-grants-2016_03