HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 54120872, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 54453222 | HCID 54453222 | — |
| Product | HCID 54120872 | HCID 54120872 | — |
Reaction Steps
4-Amino-5-chloro-2-methoxy-N-((1-(6-(4-methylbenzylamino)hexyl)-piperidin-4-yl)methyl)benzamide (0.77 g) as starting compound, acetaldehyde (0.1 ml) and sodium cyanoborohydride (0.23 g) were reacted and treated in the same manner as in Example 136 to give 0.42 g of 4-amino-5-chloro-N-((1-(6-(N-ethyl-N-(4-methylbenzyl)amino)hexyl)-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-28649560379346949cad66b63e8d2dbb |
| Source note | uspto-grants-1999_01 |