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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171813Generated: October 29, 2026

1,2-Dichloroethane → HCID 118023955, compound

https://huagongshe.com/reaction/2171813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1H-Benzotriazole-1-methanolHCID 224169—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 118023935HCID 118023935—
SolventWaterHCID 962—
ProductHCID 118023955HCID 118023955—

Reaction Steps

To a mixture of 2-[(6-cyclohexyl-2-methylthieno[2,3-d]pyrimidin-4-yl)methyl]-2,5-diazabicyclo[2.2.2]octan-3-one (67 mg), 1H-benzotriazole-1-methanol (54 mg), and DCE was added NaBH(OAc)3 (115 mg) at room temperature, followed by stirring at the same temperature for 5 hours. To the reaction mixture was added water, followed by extraction with EtOAc. The organic layer was washed with brine, dried over Na2SO4, and then concentrated under reduced pressure. The residue was purified by basic silica gel column (hexane/EtOAc) and the obtained purified product was dissolved in EtOAc. An excess amount of 4 M HCl/EtOAc was added thereto, followed by concentration under reduced pressure. To the residue was added Et2O, followed by stirring, and the precipitate was collected by filtration to obtain 2-[(6-cyclohexyl-2-methylthieno[2,3-d]pyrimidin-4-yl)methyl]-5-methyl-2,5-diazabicyclo[2.2.2]octan-3-one hydrochloride (57 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051339B2
Source datasetuspto-grants-2015_06
ORD IDord-a374e7aa34b14f028f6f0e2b5a70a4a7
Source noteuspto-grants-2015_06