HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxybenzaldehyde → HCID 57860877, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57860799 | HCID 57860799 | — |
| Reactant | HCID 68533874 | HCID 68533874 | — |
| Product | HCID 57860877 | HCID 57860877 | — |
Reaction Steps
Using methods substantially equivalent to those described in Example 94-E except that sodium borohydride was the reducing agent, 2-[4-methoxy-2-[3-(2-methoxybenzyl)-aminopropoxy]benzoylamino]-N-(4-methoxyphenyl)-4-nitrobenzamide (52 mg, 0.085 mmol, 56%) was prepared from 2-[2-(3-aminopropoxy)-4-methoxybenzoylamino]-N-(4-methoxyphenyl)-4-nitrobenzamide and 2-methoxybenzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700628B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-88bd00d86c1b449084999e2d4062e568 |
| Source note | uspto-grants-2010_04 |