Aluminum(III) Chloride → (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate

HRID 717037Notes

Reaction equation

HRID 717037 reaction equation
C([N:8]1[C:17]2[C:12](=[CH:13][C:14]([C:18]([O:20][CH3:21])=[O:19])=[CH:15][CH:16]=2)[N:11]=[C:10]([N:22]2[CH2:26][CH2:25][CH2:24][C@@H:23]2[CH3:27])[C:9]1=[O:28])C1C=CC=CC=1.[Al+3].[Cl-].[Cl-].[Cl-]>ClCCl>[CH3:27][C@H:23]1[CH2:24][CH2:25][CH2:26][N:22]1[C:10]1[C:9](=[O:28])[NH:8][C:17]2[C:12]([N:11]=1)=[CH:13][C:14]([C:18]([O:20][CH3:21])=[O:19])=[CH:15][CH:16]=2

Participants

4

Conditions

Temperature
30 °C

Procedure

Into a 250-mL round-bottom flask, was placed a solution of (S)-methyl 1-benzyl-3-(2-methylpyrrolidin-1-yl)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate (2.2 g, 5.84 mmol, 1.00 equiv) in dichloromethane (100 mL). This was followed by the addition of AlCl3 (7.7 g, 58.33 mmol, 10.00 equiv) in several batches. The resulting solution was stirred overnight at 30° C. in an oil bath. The resulting solution was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (1:100). This resulted in 900 mg (53%) of (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate as a brown solid.

Workup

  1. customInto a 250-mL round-bottom flask, was placed
  2. concentrationThe resulting solution was concentrated under vacuum
  3. customThis resulted in 900 mg (53%) of (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate as a brown solid

Sources & evidence

ORD record
ord-0c18c5e28d9c4dafbc3b8387957b3062
Source dataset
uspto-grants-2015_11
Patent number
US09193693B2

Reaction notes

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