HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851285Generated: October 31, 2026
Sodium Bicarbonate → 2-{1-[4-(2-Methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)benzyl]-piperidine-4-yl}-quinoxaline
https://huagongshe.com/reaction/1851285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-(Piperidin-4-yl)quinoxaline | HCID 21198026 | — |
| Reactant | 4-(2-Methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)benzaldehyde | HCID 86703034 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-{1-[4-(2-Methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)benzyl]-piperidine-4-yl}-quinoxaline | HCID 68751025 | — |
Reaction Steps
219.2 mg (0.76 mmol) 2-Piperidine-4-ylquinoxaline are dissolved in 5.5 mL NMP. After addition of 0.2 mL triethylamine the reaction mixture is stirred for one hour. 200 mg (0.64 mmol) 4-(2-Methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)benzaldehyde and 0.06 mL acetic acid are added. The reaction mixture is stirred overnight at room temperature. 148 mg (0.7 mmol) NaBH(OAc)3, are added in portions and the reaction mixture is stirred at room temperature for 18 hours. Additionally 75 mg NaBH(OAc)3 and 0.03 mL acetic acid are added and the stirring is continued for four days. The reaction mixture is treated with saturated NaHCO3 and vigorously stirred for one hour. The precipitate is filtered off, washed with water and dried. This solid is treated three times with each 20 mL dichloromethane. After filtration of the combined dichloromethane extracts the filtrate is evaporated and the residue purified by chromatography on silica gel (dichloromethane/methanol). After an additional purification by HPLC 84 mg (25.8%) of the pure product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957064B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-53265d67b7f94b3494bee656be7af6ec |
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| Source note | uspto-grants-2015_02 |
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