HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059589Generated: November 3, 2026
Water → 6-(azepan-4-yloxy)-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one
https://huagongshe.com/reaction/2059589
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Azepan-4-ol | HCID 5149746 | — |
| Reactant | 6-fluoro-2-(4-methoxybenzyl)-7-methylisoquinolin-1(2H)-one | HCID 59226043 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 6-(azepan-4-yloxy)-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one | HCID 68555812 | 41% |
Reaction Steps
A solution of 58 mg (0.51 mmol) azepan-4-ol in 5 ml dimethylacetamide was stirred with 45 mg (1.52 mmol) 80 percent sodium hydride for 45 minutes at room temperature. Then 150 mg (0.51 mmol) 6-fluoro-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one in dimethylacetamide was added. The reaction mixture was heated to 80° C. for 3 days during which additional amounts of azepan-4-ol and sodium hydride were added until complete conversion of the 6-fluoro-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one was obtained. The reaction mixture was slowly added to 10 ml water and after 1 h of stirring the product was isolated by filtration and dried overnight in vacuum. 82 mg of 6-(azepan-4-yloxy)-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278294B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-e58dfde0a0374274af02074f24a4e936 |
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| Source note | uspto-grants-2012_10 |
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