Hydrochloric Acid → N-(7-chloro-6-(2-fluoro-4-iodophenylamino)-3-methyl-3a,7a-dihydro-3H-imidazo[4,5-b]pyridin-5-yl)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide

HRID 1161811Notes

Reaction equation

HRID 1161811 reaction equation
[Si]([O:8][CH2:9][CH2:10][C:11]1([S:14]([NH:17][C:18]2[C:19]([NH:29][C:30]3[CH:35]=[CH:34][C:33]([I:36])=[CH:32][C:31]=3[F:37])=[C:20]([Cl:28])[CH:21]3[N:26]=[CH:25][N:24]([CH3:27])[CH:22]3[N:23]=2)(=[O:16])=[O:15])[CH2:13][CH2:12]1)(C(C)(C)C)(C)C.Cl>C1COCC1>[Cl:28][C:20]1[CH:21]2[N:26]=[CH:25][N:24]([CH3:27])[CH:22]2[N:23]=[C:18]([NH:17][S:14]([C:11]2([CH2:10][CH2:9][OH:8])[CH2:13][CH2:12]2)(=[O:16])=[O:15])[C:19]=1[NH:29][C:30]1[CH:35]=[CH:34][C:33]([I:36])=[CH:32][C:31]=1[F:37]

Participants

4

Procedure

To a solution of 1-(2-(tert-butyldimethylsilyloxy)ethyl)-N-(7-chloro-6-(2-fluoro-4-iodophenylamino)-3-methyl-3a,7a-dihydro-3H-imidazo[4,5-b]pyridin-5-yl)cyclopropane-1-sulfonamide (40 mg, 0.060 mmol) in THF (2 ml) is added HCl (0.20 ml, 1.2 N in H2O, 0.24 mmol). After stirring for 1 h, the reaction is quenched with saturated aqueous NaHCO3 solution (3 ml) and extracted with EtOAc (2×10 ml). The combined organic solution is dried over Na2SO4 and concentrated. Silica gel chromatography yields the title compound.

Workup

  1. customthe reaction is quenched with saturated aqueous NaHCO3 solution (3 ml)
  2. extractionextracted with EtOAc (2×10 ml)
  3. dry with materialThe combined organic solution is dried over Na2SO4
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-709195d314044175ab23e0b0649224cb
Source dataset
uspto-grants-2010_10
Patent number
US07820664B2

Reaction notes

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