HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 54366507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 53944756 | HCID 53944756 | — |
| Product | HCID 54366507 | HCID 54366507 | — |
Reaction Steps
4-Amino-5-chloro-2-methoxy-N-((1-(6-(2-thienylmethylamino)hexyl)-piperidin-4-yl)methyl)benzamide (0.8 g) as starting compound, acetaldehyde (0.12 ml) and sodium cyanoborohydride (0.26 g) were reacted and treated in the same manner as in Example 136 to give 0.8 g of 4-amino-5-chloro-N-((1-(6-(N-ethyl-N-(2-thienylmethyl)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-2b250dbaddf54d00905f455131843a9c |
| Source note | uspto-grants-1999_01 |