p-Bromobenzenesulfonyl chloride → 4-bromo-N-((1R,2R)-2-methylcyclopropyl)benzenesulfonamide

HRID 2091586Notes

Reaction equation

HRID 2091586 reaction equation
[CH3:1][C@@H:2]1[CH2:4][C@H:3]1[NH:5]C(=O)OCC1C=CC=CC=1.C(N(CC)CC)C.[Br:23][C:24]1[CH:29]=[CH:28][C:27]([S:30](Cl)(=[O:32])=[O:31])=[CH:26][CH:25]=1>C(Cl)Cl.[Pd]>[Br:23][C:24]1[CH:29]=[CH:28][C:27]([S:30]([NH:5][C@@H:3]2[CH2:4][C@H:2]2[CH3:1])(=[O:32])=[O:31])=[CH:26][CH:25]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

A solution of benzyl ((1R,2R)-2-methylcyclopropyl)carbamate (1.68 g, 8.2 mmol) in DCM (55 mL) was charged with 10 wt % Pd/C, then degassed and charged with hydrogen (50 PSI). The reaction was complete after 30 min and so was filtered over celite, rinsing with DCM (15 mL). The liquor was cooled to 0° C., and treated with triethylamine (3.43 mL, 24.6 mmol) and 4-bromobenzene-1-sulfonyl chloride (2.20 g, 8.61 mmol). The cold bath was removed and the reaction was stirred for 1 h. At completion, the reaction was washed with 0.5 M aq. HCl (2×20 mL) and brine (20 mL), dried over MgSO4 and concentrated to provide 4-bromo-N-((1R,2R)-2-methylcyclopropyl)benzenesulfonamide (2.06 g, 87% yield). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.74-7.80 (m, 1H), 7.66-7.72 (m, 1H), 4.90 (br. s., 1H), 1.94 (dt, J=3.5, 1.8 Hz, 1H), 1.41 (t, J=7.3 Hz, 1H), 0.89-1.01 (m, 3H), 0.70-0.81 (m, 1H), 0.35-0.45 (m, 1H).

Workup

  1. customdegassed
  2. additioncharged with hydrogen (50 PSI)
  3. filtrationso was filtered over celite
  4. washrinsing with DCM (15 mL)
  5. customThe cold bath was removed
  6. washAt completion, the reaction was washed with 0.5 M aq. HCl (2×20 mL) and brine (20 mL)
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-1a7b9b0dc49b42f0b9394e8016714926
Source dataset
uspto-grants-2013_05
Patent number
US08440652B2

Reaction notes

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