Hydrochloric Acid → HCID 57619388, compound

HRID 1367368Notes

Reaction equation

HRID 1367368 reaction equation
C(OC(=O)[N:7]([CH2:24][C:25]1[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=1)[C:8]1[S:9][C:10]([C:13]([C:15]2[C:23]3[C:18](=[N:19][CH:20]=[CH:21][CH:22]=3)[NH:17][CH:16]=2)=[O:14])=[CH:11][N:12]=1)(C)(C)C.Cl.C(=O)(O)[O-].[Na+]>ClCCl>[F:31][C:28]1[CH:29]=[CH:30][C:25]([CH2:24][NH:7][C:8]2[S:9][C:10]([C:13]([C:15]3[C:23]4[C:18](=[N:19][CH:20]=[CH:21][CH:22]=4)[NH:17][CH:16]=3)=[O:14])=[CH:11][N:12]=2)=[CH:26][CH:27]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 57619372HCID 57619372, compound

Product 1

HCID 57619388HCID 57619388, compoundYield 12.8%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of (4-fluoro-benzyl)-[5-(1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-thiazol-2-yl]-carbamic acid tert-butyl ester (549, 0.11 g, 0.2 mmol) in dichloromethane (2 mL) was added hydrogen chloride (4 M in 1,4-dioxane, 2 mL). The reaction mixture was stirred at room temperature overnight. The reaction mixture was poured into cold sodium bicarbonate solution, extracted with ethyl acetate, washed with brine and dried over magnesium sulfate. After removal of solvents, the residue was washed with ethyl acetate to provide the desired compound as a yellow solid (P-0177, 9 mg, 10%). MS (ESI) [M+H+]+=353.12.

Workup

  1. extractionextracted with ethyl acetate
  2. washwashed with brine
  3. dry with materialdried over magnesium sulfate
  4. customAfter removal of solvents
  5. washthe residue was washed with ethyl acetate

Sources & evidence

ORD record
ord-bd40315dbc144456b46a32a92bd1c3ef
Source dataset
uspto-grants-2011_02
Patent number
US07893075B2

Reaction notes

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