HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-tert-Butylethylamine → 3-acetyl-2-(N-tert-butyl-N-ethylaminomethyl)-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-tert-Butylethylamine | HCID 521156 | — |
| Reactant | 3-Acetyl-2-bromomethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline | HCID 19039905 | — |
| Product | 3-acetyl-2-(N-tert-butyl-N-ethylaminomethyl)-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline | HCID 19039892 | — |
Reaction Steps
According to the same manner as that described in Example 1, 3-acetyl-2-bromomethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline was reacted with N-tert-butyl-N-ethylamine to give 3-acetyl-2-(N-tert-butyl-N-ethylaminomethyl)-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline. This compound was recrystallized from methanol to give colorless prisms. mp. 156°-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05641788 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-447b0500dc8041a6b7c2679632aa0387 |
| Source note | uspto-grants-1997_06 |