4-Chlorobenzenesulfonyl chloride → HCID 25263461, compound

HRID 1375197Notes

Reaction equation

HRID 1375197 reaction equation
[CH3:1][C:2]([C@H:5]([NH2:8])[CH2:6][OH:7])([CH3:4])[CH3:3].C(N(CC)CC)C.[Cl:16][C:17]1[CH:22]=[CH:21][C:20]([S:23](Cl)(=[O:25])=[O:24])=[CH:19][CH:18]=1>C(Cl)Cl>[Cl:16][C:17]1[CH:22]=[CH:21][C:20]([S:23]([NH:8][C@H:5]([CH2:6][OH:7])[C:2]([CH3:4])([CH3:3])[CH3:1])(=[O:25])=[O:24])=[CH:19][CH:18]=1

Participants

5

Procedure

To a solution of S-tert-leucinol (0.20 g, 1.70 mmol), triethylamine (0.19 g, 1.87 mmol) and methylene chloride (10 mL) at 0° C., was added a solution of 4-chloro benzenesulfonyl chloride (0.36 g, 1.70 mmol) in CH2Cl2 (5 mL). After 15 minutes the ice bath was removed and the reaction allowed to reach 25° C. After 16 hours, the reaction was quenched by pouring into saturated sodium bicarbonate solution (20 mL) and additional-methylene chloride (15 mL). The organic phase was separated and washed sequentially with 1N HCl solution (20 mL), distilled water and brine, dried over MgSO4 and evaporated to give the desired product as a white solid, mp 128-130° C. (0.46 g, 94%). MS (+APCI) 292.06 ([M+H]+). Anal. Calc'd for C12H18ClNO3S: C, 49.39; H, 6.22; N, 4.80; Found: C, 49.40; H, 6.17; N, 4.79.

Workup

  1. customAfter 15 minutes the ice bath was removed
  2. customto reach 25° C
  3. customthe reaction was quenched
  4. additionby pouring into saturated sodium bicarbonate solution (20 mL)
  5. customThe organic phase was separated
  6. washwashed sequentially with 1N HCl solution (20 mL)
  7. distillationdistilled water and brine
  8. dry with materialdried over MgSO4
  9. customevaporated

Sources & evidence

ORD record
ord-c9baa03ff36e4b3b85af6cf280c51b1d
Source dataset
uspto-grants-2007_01
Patent number
US07166622B2

Reaction notes

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