Water → 2-(1,2,3,7,8,9-Hexahydroindeno[5,4-b][1,4]oxazin-9-yl) ethylamine

HRID 324650Notes

Reaction equation

HRID 324650 reaction equation
[NH2:1][CH2:2][CH2:3][CH:4]1[C:16]2[C:15]3[NH:14][C:13](=O)[CH2:12][O:11][C:10]=3[CH:9]=[CH:8][C:7]=2[CH2:6][CH2:5]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[NH:14]1[CH2:13][CH2:12][O:11][C:10]2[CH:9]=[CH:8][C:7]3[CH2:6][CH2:5][CH:4]([CH2:3][CH2:2][NH2:1])[C:16]=3[C:15]1=2

Participants

6

Procedure

A solution of 9-(2-aminoethyl)-1,7,8,9-tetrahydroindeno[5,4-b][1,4]oxazin-2(3H)-one (1.2 g, 5.3 mmol.) in tetrahydrofuran (30 mL) was was cooled with ice, to which was added lithium aluminum hydride (0.8 g, 21.4 mmol.). The mixture was heated for 18 hours under reflux under argon atmosphere. The reaction mixture was cooled, to which were added water (0.8 mL), a 15% aqueous solution of sodium hydroxide (0.8 mL) and water (2.4 mL), successively. The mixture was then stirred for 30 minutes at room temperature. Insolubles were filtered off, and the filtrate was concentrated under reduced pressure. Then, in substantially the same manner as in Example 36, from 2-(1,2,3,7,8,9-hexahydroindeno[5,4-b][1,4]oxazin-9-yl) ethylamine thus obtained and propionic acid, the title compound was produced (yield 250 mg, 51%).

Workup

  1. temperatureThe mixture was heated for 18 hours
  2. temperatureunder reflux under argon atmosphere
  3. temperatureThe reaction mixture was cooled, to which
  4. filtrationInsolubles were filtered off
  5. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-b32d065af6fc4e37bf880c74a8f9553f
Source dataset
uspto-grants-2001_04
Patent number
US06218429B1

Reaction notes

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