Reaktion #496382

Reaktionsgleichung

1-cyano-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester

glycine

sodium methoxide

→

title compound

Ausbeute 97.4%

[(1-Cyano-4-hydroxy-8-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid

Ausbeute 97.4%

Lösungsmittel

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Einengenconcentrated in vacuo
2. 2
   workup.ADDITIONWater (75 mL) was added
3. 3
   SonstigeA clear yellow solution was obtained after 5 minutes of sonication
4. 4
   WaschenThe solution was washed with dichloromethane (2×50 mL)
5. 5
   SonstigeThe white precipitate formed
6. 6
   Sonstigewas separated by filtration
7. 7
   Waschenwashed with water
8. 8
   Sonstigedried in vacuo

Vorschrift

A mixture of 1-cyano-4-hydroxy-8-phenoxy-isoquinoline-3-carboxylic acid methyl ester (322 mg, 1.0 mmol), glycine (1.51 g, 20.1 mmol), and a 0.5 M sodium methoxide solution in methanol (38.2 mL) was refluxed for 31 h before it was cooled to room temperature and concentrated in vacuo. Water (75 mL) was added and the pH of the yellow suspension was adjusted to 10 with aqueous 1 N HCl. A clear yellow solution was obtained after 5 minutes of sonication. The solution was washed with dichloromethane (2×50 mL). The remaining aqueous layer was acidified to pH=3 with aqueous 1 N HCl. The white precipitate formed was separated by filtration, washed with water and dried in vacuo to give the title compound as a white solid (354 mg): 1H NMR (DMSO-d6, 200 MHz): δ=12.86 (bs, 1H), 9.56 (t, 1H), 8.09 (m, 1H), 7.88 (t, J=8.2 Hz, 1H), 7.47 (m, 2H), 7.21 (m, 4H), 4.05 (d, J=5.8 Hz, 2H).

Quelle