HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171813Generated: October 29, 2026
1,2-Dichloroethane → HCID 118023955, compound
https://huagongshe.com/reaction/2171813
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1H-Benzotriazole-1-methanol | HCID 224169 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 118023935 | HCID 118023935 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 118023955 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051339B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-a374e7aa34b14f028f6f0e2b5a70a4a7 |
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| Source note | uspto-grants-2015_06 |
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