Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 21278384 | HCID 21278384 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14326774 | HCID 14326774 | 71% |
Reaction Steps
To 50 ml of dichloromethane were added 4.0 g of the thus obtained 1-(1-chloro-5-isoquinolinesulfonyl)-4-p-toluenesulfonyloxypiperidine and 1 ml of a 40% methylamine solution in methanol. The mixture was heated at 70° C. for 6 hours in a sealed vessel. Then, the dichloromethane was removed under reduced pressure to obtain an oily residue. The thus obtained oily residue was subjected to purification by silica gel column chromatography (Wacogel C-200, 100 g; solvent: a 5% methanol solution in chloroform) to obtain 2.28 g of 1-(1-chloro-5-isoquinolinesulfonyl)-4-methylaminopiperidine [Compound (94)] in a yield of 71%. Compound (94) was analyzed to give the following data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04798897 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-2ca7804284954d6ebd6c7967dfe7d132 |
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| Source note | uspto-grants-1989_01 |
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