p-Toluenesulfonic acid → 7-Bromo-6-[3-bromo-2-(1-ethoxyethoxy)-propoxy]-1-[2-(tert-butyldimethyl-silanyloxy)-propyl]-1H-indazole

HRID 1815956Notes

Reaction equation

HRID 1815956 reaction equation
[Br:1][CH2:2][CH:3]([OH:27])[CH2:4][O:5][C:6]1[C:14]([Br:15])=[C:13]2[C:9]([CH:10]=[N:11][N:12]2[CH2:16][CH:17]([O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21])[CH3:18])=[CH:8][CH:7]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1.[CH:39]([O:41][CH2:42][CH3:43])=[CH2:40]>ClCCl>[Br:15][C:14]1[C:6]([O:5][CH2:4][CH:3]([O:27][CH:39]([O:41][CH2:42][CH3:43])[CH3:40])[CH2:2][Br:1])=[CH:7][CH:8]=[C:9]2[C:13]=1[N:12]([CH2:16][CH:17]([O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:21])[CH3:22])[CH3:18])[N:11]=[CH:10]2

Participants

5

Procedure

To a solution of the product from Step E (3.78 g, 7.2 mmol) and p-toluenesulfonic acid (0.14 g) in dichloromethane (50 mL) at 0° C. was added ethyl vinyl ether (2.75 mL, 28.8 mmol). After 30 min the reaction was quenched with a saturated solution of sodium bicarbonate (50 mL) and the mixture was extracted with dichloromethane (3×80 mL). Evaporation and purification by chromatography (silica, 1% to 8% EtOAc/hexane) gave a viscous oil (3.30 g, 77%): LC/MS (+APCI) m/z 593, 595, 597 (M+H).

Workup

  1. customAfter 30 min the reaction was quenched with a saturated solution of sodium bicarbonate (50 mL)
  2. extractionthe mixture was extracted with dichloromethane (3×80 mL)
  3. customEvaporation and purification by chromatography (silica, 1% to 8% EtOAc/hexane)

Sources & evidence

ORD record
ord-7ef6e46384ca442ba3cb7b5f61694609
Source dataset
uspto-grants-2005_04
Patent number
US06881749B2

Reaction notes

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