HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 54391210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 53745440 | HCID 53745440 | — |
| Product | HCID 54391210 | HCID 54391210 | — |
Reaction Steps
4-Amino-N-((1-(4-benzylaminobutyl)piperidin-4-yl)methyl)-5-chloro-2-methoxybenzamide (0.5 g) as starting compound, acetaldehyde (0.07 ml) and sodium cyanoborohydride (0.15 g) were reacted and treated in the same manner as in Example 136 to give 0.35 g of 4-amino-5-chloro-N-((1-(4-(N-ethyl-N-benzylamino)butyl)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-2f3094930e6d4f809e4688fa578dbebe |
| Source note | uspto-grants-1999_01 |