HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930215Generated: November 2, 2026
Acetic Acid → 7-Chloro-6-(1-isopropyl-piperidin-4-yloxy)-2H-isoquinolin-1-one
https://huagongshe.com/reaction/1930215
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 7-Chloro-6-(piperidin-4-yloxy)-2h-isoquinolin-1-one-hydro-chloride | HCID 67458042 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Chloro-6-(1-isopropyl-piperidin-4-yloxy)-2H-isoquinolin-1-one | HCID 57652499 | 17.6% |
Reaction Steps
64 mg (0.23 mmol) of 7-chloro-6-(piperidin-4-yloxy)-2H-isoquinolin-1-one-hydro-chloride (54) were dissolved in 5 mL of methanol. 41.4 mg (0.41 mmol) of triethyl amine were added and the mixture stirred at room temperature for 10 minutes. After adding freshly dried molecular sieves, 122.4 mg (2.04 mmol) acetic acid, 26.7 mg (0.46 mmol) of acetone and 43.3 mg (0.69 mmol) of sodium cyanoborohydride, the reaction mixture was refluxed for 8 h. After the addition of 2 equivalents acetone and 2 equivalents of sodium cyanoborohydride at room temperature, the reaction was refluxed for another 2 h to complete conversion. For working up, the mixture was filtered and the filtrate was evaporated. The residue was dissolved in dichloromethane, washed twice with 2 N NaOH and water and dried over MgSO4. After evaporation of the solvent and purification by preparative HPLC, 13 mg of the title compound were obtained as trifluoroacetate. Rt=0.96 min (Method B). Detected mass: 321.1/323.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188117B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-e4feee1783b7402e9b1a5deba1085ff7 |
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| Source note | uspto-grants-2012_05 |
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