Dimethylamine → HCID 10777845, compound

HRID 234278Notes

Reaction equation

HRID 234278 reaction equation
[CH3:1][C:2]1([CH2:14][C:15]([OH:17])=O)[CH2:6][C:5]2[C:7]([CH3:13])=[CH:8][C:9]([CH3:12])=[C:10]([CH3:11])[C:4]=2[O:3]1.O.ON1C2C=CC=CC=2N=N1.Cl.[CH2:30]([N:32]=[C:33]=NCCCN(C)C)C.CNC>CN(C)C=O.O>[CH3:30][N:32]([CH3:33])[C:15](=[O:17])[CH2:14][C:2]1([CH3:1])[CH2:6][C:5]2[C:7]([CH3:13])=[CH:8][C:9]([CH3:12])=[C:10]([CH3:11])[C:4]=2[O:3]1

Participants

7

Procedure

To a solution of 2,4,6,7-tetramethyl-2,3-dihydrobenzofuran-2-yl acetic acid (3.0 g, 12.8 mmol) in dimethylformamide (30 ml) were added 1-hydroxy-1H-benzotriazole monohydrate (HOBt) (2.1 g, 14.1 mmol) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (WSC) (3.7 g, 19.2 mmol). The mixture was stirred at room temperature for 1 hour. Then, 50% dimethylamine aqueous solution (3 ml) was added and the resulting mixture was stirred for additional 30 minutes. The reaction mixture was diluted with water and the product was extracted with ethyl acetate. The extract was washed with water, dried and concentrated. The residue was purified by column chromatography on silica gel (isopropyl ether) to obtain the desired compound (3.1 g, yield: 92.6% yield) as oil.

Workup

  1. stirringthe resulting mixture was stirred for additional 30 minutes
  2. extractionthe product was extracted with ethyl acetate
  3. washThe extract was washed with water
  4. customdried
  5. concentrationconcentrated
  6. customThe residue was purified by column chromatography on silica gel (isopropyl ether)

Sources & evidence

ORD record
ord-589dc2fae93a45e59e74a1c152564e07
Source dataset
uspto-grants-1997_01
Patent number
US05594154

Reaction notes

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