Pyridine → HCID 59267946, compound

HRID 1802372Notes

Reaction equation

HRID 1802372 reaction equation
[Na+].[S:2]1[C:6]2[CH:7]=[C:8]([S:11]([O-:13])=[O:12])[CH:9]=[CH:10][C:5]=2[N:4]=[CH:3]1.N1C=CC=CC=1.Br[C:21]([CH3:28])([CH3:27])[C:22]([O:24][CH2:25][CH3:26])=[O:23]>CN(C=O)C>[CH2:25]([O:24][C:22](=[O:23])[C:21]([S:11]([C:8]1[CH:9]=[CH:10][C:5]2[N:4]=[CH:3][S:2][C:6]=2[CH:7]=1)(=[O:13])=[O:12])([CH3:28])[CH3:27])[CH3:26]

Participants

5

Reactant 3

HCID 1049PyridineHCID 11745Propanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 67122946HCID 67122946, compound

Product 1

HCID 59267946HCID 59267946, compoundYield 66%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
50 °C

Procedure

The crude 1,3-benzothiazol-6-sulfinic acid sodium salt (1.1 g, 4.97 mmol) is suspended in DMF (15 mL). Pyridine (0.33 mL) and ethyl α-bromoisobutyrate (0.61 mL) are added. The reaction is stirred at 50° C. under nitrogen for 2 h. The reaction mixture is cooled to room temperature and the solvent is removed under reduced pressure. The residue is dissolved in ethyl acetate (20 mL) and washed with 2M aqueous HCl solution (20 mL). The acidic aqueous layer is back-extracted with ethyl acetate (2×20 mL). The combined organic extracts are washed with brine (20 mL) and dried over Na2SO4. Filtration, concentration under reduced pressure, followed by column chromatography of the residue (silica, eluent DCM, 30-40% ethyl acetate) afforded 0.85 g of 2-(benzothiazole-6-sulfonyl)-2-methyl-propionic acid ethyl ester. Yield: 66%, ES-MS: m/z 314 [M+H]; 1H NMR (250 MHz, CHLOROFORM-d) δ ppm 1.19 (3 H, t, J=7.16 Hz), 1.67 (6 H, s), 4.15 (2 H, q, J=7.13 Hz), 7.99 (1 H, dd, J=8.68, 1.79 Hz), 8.28 (1H, d, J=8.68 Hz), 8.54 (1 H, d, J=1.48 Hz), 9.26 (1 H, s);

Workup

  1. temperatureThe reaction mixture is cooled to room temperature
  2. customthe solvent is removed under reduced pressure
  3. dissolutionThe residue is dissolved in ethyl acetate (20 mL)
  4. washwashed with 2M aqueous HCl solution (20 mL)
  5. extractionThe acidic aqueous layer is back-extracted with ethyl acetate (2×20 mL)
  6. washThe combined organic extracts are washed with brine (20 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationFiltration, concentration under reduced pressure

Sources & evidence

ORD record
ord-b0675e5b5e1947c8b5271a28b462d487
Source dataset
uspto-grants-2013_01
Patent number
US08349871B2

Reaction notes

Loading…