HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dimethylpyridine → HCID 12021108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dimethylpyridine | HCID 11565 | — |
| Reactant | 3-(CHLOROMETHYL)-5-METHYLPYRIDINE | HCID 11962782 | — |
| Reactant | 10-bromo-5-hydroxy-2-(3-pyridylmethyl)-3H-pyrido[3,2,1-kl]phenothiazin-3-one | HCID 12021105 | — |
| Product | HCID 12021108 | HCID 12021108 | 10% |
Reaction Steps
According to Example 34, the compound (150 mg) produced in Example 37 was reacted with 3-chloromethyl-5-methylpyridine synthesized from 3,5-dimethylpyridine (500 mg) to obtain the title compound (180 mg; 10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476021B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-0cf8adf304a04477a2c3f3240faebc3a |
| Source note | uspto-grants-2002_11 |