Water → (S)-1-(7-methoxy-1,4-dihydro-indeno[1,2-b]pyrrol1-yl)-propan-2-ol

HRID 264450Notes

Reaction equation

HRID 264450 reaction equation
O=[CH:2][CH2:3][CH:4]1[CH2:12][C:11]2[C:6](=[CH:7][C:8]([O:13][CH3:14])=[CH:9][CH:10]=2)[C:5]1=O.O.[NH2:17][CH2:18][C@@H:19]([OH:21])[CH3:20]>C1(C)C=CC=CC=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>[CH3:14][O:13][C:8]1[CH:7]=[C:6]2[C:11]([CH2:12][C:4]3[CH:3]=[CH:2][N:17]([CH2:18][C@@H:19]([OH:21])[CH3:20])[C:5]=32)=[CH:10][CH:9]=1

Participants

6

Reactant 3

HCID 962WaterHCID 7311736(S)-(+)-1-Aminopropan-2-olHCID 10703357(RS)-2-(2-oxoethyl)-6-methoxy-1-indanone

Product 1

HCID 10847817(S)-1-(7-methoxy-1,4-dihydro-indeno[1,2-b]pyrrol1-yl)-propan-2-olYield 63%

Reagents, catalysts & solvents 2

HCID 6101p-Toluenesulfonic acidCatalystHCID 1140TolueneSolvent2×

Procedure

A solution of 2 g of (RS)-2-(2-oxoethyl)-6-methoxy-1-indanone and 80 mg of p-toluenesulfonic acid in 70 ml of anhydrous toluene was heated on a water separator. A solution of 2.94 g of (S)-1-amino-2-propanol in 20 ml of anhydrous toluene was added dropwise to the boiling solution over a period of 5 minutes. Subsequently, the mixture was boiled for an additional 30 minutes, during which the solvent was reduced to a volume of 20 ml. The cooled reaction mixture was purified by column chromatography on silica gel (ethyl acetate/toluene 1:1). 1.5 g (63%) of (S)-1-(7-methoxy-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol were obtained as a solid with m.p. 74°.

Workup

  1. customThe cooled reaction mixture
  2. customwas purified by column chromatography on silica gel (ethyl acetate/toluene 1:1)

Sources & evidence

ORD record
ord-e238ab2cb67f4a4a97ac95f252580e1a
Source dataset
uspto-grants-1997_07
Patent number
US05646173

Reaction notes

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