HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → HCID 14326747, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 14326757 | HCID 14326757 | — |
| Reactant | HCID 21278403 | HCID 21278403 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14326747 | HCID 14326747 | — |
Reaction Steps
Substantially the same procedures as in Example 13 were repeated except that 5.84 g to 1-(5-isoquinolinesulfonyl)-3-hydroxypiperidine was used in place of 5.84 g of 1-(5-isoquinolinesulfonyl)-4-hydroxypiperidine and that 2.9 g of the thus obtained 1-(5-isoquinolinesulfonyl)-3-piperidone was reacted in methanol with 2.31 g of ammonium acetate and 0.63 g of sodium cyanoborohydride at 20° C. for 24 hours. There was obtained 2.37 g of 1-(5-isoquinolinesulfonyl)-3-aminopiperidine [Compound(63)]. Compound (63) was analyzed to give the following data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04798897 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-727c52b93f0f41738ca74785778b16f2 |
| Source note | uspto-grants-1989_01 |