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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171825Generated: November 2, 2026

1,2-Dichloroethane → HCID 118023873, compound

https://huagongshe.com/reaction/2171825

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantGlycolaldehyde dimerHCID 186078—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 118023960HCID 118023960—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 118023873HCID 11802387345.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of N-{[6-(4,4-dimethylcyclohexyl)-2-methylthieno[2,3-d]pyrimidin-4-yl]methyl}tetrahydro-2H-pyran-4-amine (100 mg), 1,4-dioxane-2,5-diol (64 mg), DCE (2 mL), and MeOH (1 mL) was added NaBH(OAc)3 (170 mg) under ice-cooling, followed by stirring at 0° C. for 1 hour. To the reaction mixture were added water and EtOAc, followed by extraction with EtOAc. The organic layer was washed with brine, dried, and then concentrated under reduced pressure. The residue was purified by silica gel column to obtain 2-[{[6-(4,4-dimethylcyclohexyl)-2-methylthieno[2,3-d]pyrimidin-4-yl]methyl}(tetrahydro-2H-pyran-4-yl)amino]ethanol (51 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051339B2
Source datasetuspto-grants-2015_06
ORD IDord-8c4025ca65d9406d985eb48d7b1a77c0
Source noteuspto-grants-2015_06