HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 54288772, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 54070614 | HCID 54070614 | — |
| Product | HCID 54288772 | HCID 54288772 | — |
Reaction Steps
4-Amino-5-chloro-N-((1-(5-cyclohexylaminopentyl)piperidin-4-yl)-methyl)-2-methoxybenzamide (1.1 g) as starting compound, acetaldehyde (0.15 ml) and sodium cyanoborohydride (0.33 g) were reacted and treated in the same manner as in Example 136 to give 1.0 g of 4-amino-5-chloro-N-((1-(5-(N-ethyl-N-cyclohexylamino)pentyl)piperidin-4-yl)methyl)-2-methoxybenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05864039 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-4fd82dcdf02548c2a5a25aaab34d0040 |
| Source note | uspto-grants-1999_01 |