HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxy-2,2-dimethylpropionaldehyde → 3-(6,7-Dimethoxyquinolin-3-yl-amino)-2,2-dimethyl-propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxy-2,2-dimethylpropionaldehyde | HCID 11699 | — |
| Reactant | HCID 10330538 | HCID 10330538 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(6,7-Dimethoxyquinolin-3-yl-amino)-2,2-dimethyl-propan-1-ol | HCID 22573178 | 21.5% |
Reaction Steps
The reaction is run similar to the preparation in Example 11. To a MeOH solution of 4 Å powdered molecular sieves (0.35 g) under argon is added 3-amino-6,7-dimethoxyquinoline (0.32 g, 1.6 mmol) and 2,2-dimethyl-3-hydroxypropionaldehyde (0.19 g, 1.9 mmol). The product mixture is chromatographed (3% MeOH/CHCl3) to afford 0.10 g of material which is partitioned between CH2Cl2/10% NaOH. The organic layer is washed with 10% NaOH, H2O, and brine, then dried (MgSO4), and recrystallized from EtOAc/hexanes to provide a light-orange solid (m.p. 170-173.5° C). Anal. Calcd. for C16H22N2O3: C, 66.18; H, 7.64; N, 9.65; Found: C, 66.11; H, 7.49; N, 9.33.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821962B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-5da4b03e9b46415f9e8d89716e427fe3 |
| Source note | uspto-grants-2004_11 |