Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 9951687 | HCID 9951687 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22121938 | HCID 22121938 | 74.6% |
Reaction Steps
To 30 ml of a suspension prepared by suspending 2.25 g of hexahydro-1-[(4-methyl-5-isoquinolinyl)sulfonyl]-1H-1,4-diazepine in pyridine was added 2.0 g of acetic anhydride, and the mixture was stirred at 60° C. for 30 minutes. This reaction mixture was concentrated, made basic with sodium hydrogencarbonate/H2O, and extracted with chloroform. The extract was dried and concentrated to provide 1.91 g of 1-acetyl-hexahydro-4-[(4-methyl-5-isoquinolinyl)sulfonyl]-1H-1,4-diazepine as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06153608 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-776d3623f7564a4391246a7fc0433d08 |
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| Source note | uspto-grants-2000_11 |
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