Water → Rac-2-(methylamino)-1-quinolin-2-ylethanol

温度

60 °C

Potassium hydroxide (3.21 g) and H2O (0.13 mL) are added to acetonitrile (50 mL). Trimethylsulfonium iodide (5.84 g) and 2-quinoline carboxaldehyde (4.50 g) are then added. The reaction mixture is heated to 60° C. for 4 h. The reaction mixture is allowed to cool to room temperature and is diluted with Et2O (25 mL) The precipitate is filtered off. 1H NMR of an aliquot of the filtrate showed mostly starting material and a small amount of the desired epoxide. The filtrate is concentrated in vacuo and the residue is re-subjected to the reaction conditions above and heated to 60° C. for 1 h. The reaction mixture is allowed to cool to room temperature and is diluted with Et2O (25 mL). The precipitate is filtered off and the filtrate is concentrated in vacuo. The resulting crude epoxide (5.5 g) is dissolved in methanol (20 mL) and added to a 2.0 M solution of methylamine in methanol (100 mL). The reaction mixture is heated to reflux for 1 h. The reaction mixture is allowed to cool to room temperature and concentrated in vacuo. The resulting brown oil is purified via column chromatography (CHCl3/methanol, 95/5, 90/10; CHCl3/methanol/NH4OH, 90/10/1) to yield 1.191 g of the title compound as a yellow-green oil.

1. temperatureto cool to room temperature
2. filtrationis filtered off
3. concentrationThe filtrate is concentrated in vacuo
4. customthe residue is re-subjected to the reaction conditions above and
5. temperatureheated to 60° C. for 1 h
6. temperatureto cool to room temperature
7. filtrationThe precipitate is filtered off
8. concentrationthe filtrate is concentrated in vacuo
9. dissolutionThe resulting crude epoxide (5.5 g) is dissolved in methanol (20 mL)
10. additionadded to a 2.0 M solution of methylamine in methanol (100 mL)
11. temperatureThe reaction mixture is heated
12. temperatureto reflux for 1 h
13. temperatureto cool to room temperature
14. concentrationconcentrated in vacuo
15. customThe resulting brown oil is purified via column chromatography (CHCl3/methanol, 95/5, 90/10; CHCl3/methanol/NH4OH, 90/10/1)

ORDレコード

ord-36d6c755d3324490b3c34566443f24f4

出典データセット

uspto-grants-2005_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06852731B2