Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 66726990 | HCID 66726990 | — |
| Product | HCID 66727106 | HCID 66727106 | — |
Reaction Steps
310 mg of p-toluenesulfonyl chloride was added to a pyridine (20 mL) solution of 510 mg of 6-(4-tert-butoxycarbonyl-1,4-diazepan-1-ylsulfonyl)isoquinoline 2-oxide obtained in Step 1 of Example 53, and the mixture was stirred at room temperature for 16 hours. Then, the reaction solvent was distilled off under reduced pressure. To the obtained residue, 9 mL of 2-ethanolamine was added, and the mixture was stirred at room temperature for 6 hours. After the completion of reaction, the reaction solution was poured into ice water, and the deposited white crystal was collected by filtration. The obtained crystal was purified by silica gel column chromatography (dichloromethane:methanol=30:1) to obtain 380 mg of the compound of interest as a white crystal (75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08951997B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-34edab09fd5e43c0b3f2898d38f30729 |
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| Source note | uspto-grants-2015_02 |
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