HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylbenzaldehyde → HCID 57860788, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylbenzaldehyde | HCID 10722 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57860799 | HCID 57860799 | — |
| Reactant | HCID 68536786 | HCID 68536786 | — |
| Product | HCID 57860788 | HCID 57860788 | — |
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-methylbenzyl)-aminopropoxy)benzoylamino]-N-(4-methoxyphenyl)-4-nitrobenzamide (50 mg, 0.084 mmol, 56%) was prepared from 2-[2-(3-aminopropoxy)-4-methoxybenzoylamino]-N-(4-methoxyphenyl)-4-nitrobenzamide and 2-methylbenzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700628B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-8e2251ba17aa4f6db3e85e255483b2d1 |
| Source note | uspto-grants-2010_04 |