HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → N-{2-methoxy-5-(5-trifluromethyltetrazole-1-yl)benzyl}-N-methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-Methoxy-5-[5-(trifluoromethyl)tetrazol-1-yl]benzaldehyde | HCID 11391618 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{2-methoxy-5-(5-trifluromethyltetrazole-1-yl)benzyl}-N-methylamine | HCID 57939583 | — |
Reaction Steps
In 40 ml of dichloromethane was dissolved 2.72 g of 2-methoxy-5-(5-trifluoromethyltetrazole-1-yl)benzaldehyde, and added thereto was 2.5 ml of 8 M methylamine in ethanol solution, 0.572 ml of acetic acid and 3.12 g of triacetoxy sodium borohydride, the mixture was stirred at room temperature for 6 hours. The reaction mixture was washed with saturated aqueous sodium hydrocarbonate solution, and the organic layers were dried and concentrate. The residue was purified by silica gel column chromatography (chloroform:methanol=49:1 to 4:1), to give 2.2 g of N-{2-methoxy-5-(5-trifluromethyltetrazole-1-yl)benzyl}-N-methylamine as shown in Table 136 below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07619092B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-373822fbb2184dc4954c487e35f9615f |
| Source note | uspto-grants-2009_11 |