Hydrochloric Acid → HCID 53628423, compound

HRID 1175539Notes

Reaction equation

HRID 1175539 reaction equation
[CH:1]1([NH2:4])[CH2:3][CH2:2]1.[F:5][C:6]1[C:32]([F:33])=[CH:31][CH:30]=[CH:29][C:7]=1[CH2:8][S:9][C:10]1[N:15]=[C:14]([NH:16][S:17]([N:20]2[CH2:25][CH2:24][C:23](=O)[CH2:22][CH2:21]2)(=[O:19])=[O:18])[CH:13]=[C:12]([O:27][CH3:28])[N:11]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+].Cl>C(Cl)Cl.C(O)(=O)C>[CH:1]1([NH:4][CH:23]2[CH2:24][CH2:25][N:20]([S:17]([NH:16][C:14]3[CH:13]=[C:12]([O:27][CH3:28])[N:11]=[C:10]([S:9][CH2:8][C:7]4[CH:29]=[CH:30][CH:31]=[C:32]([F:33])[C:6]=4[F:5])[N:15]=3)(=[O:18])=[O:19])[CH2:21][CH2:22]2)[CH2:3][CH2:2]1

Participants

8

Reactant 5

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 69828CyclopropylamineHCID 5049666Sodium triacetoxyborohydrideHCID 67051257HCID 67051257, compound

Product 1

HCID 53628423HCID 53628423, compound

Reagents, catalysts & solvents 2

HCID 176Acetic AcidSolventHCID 6344DichloromethaneSolvent2×

Procedure

A solution of cyclopropylamine (0.08 mL) in DCM (2 mL) was added to a solution of acetic acid (0.025 mL) and N-{2-[(2,3-difluorobenzyl)thio]-6-methoxypyrimidin-4-yl}-4-oxopiperidine-1-sulfonamide (the product of example 148, step iii) (0.10 g) in DCM (2 mL). The solution was stirred at room temperature for 1 h then sodium triacetoxyborohydride (0.24 g) was added in portions. The mixture was stirred at room temperature overnight then 3M aqueous sodium hydroxide (6 mL) added to the residue. The mixture was shaken vigorously then acidified to pH 8 with 2M aqueous hydrochloric acid and extracted with ethyl acetate. The combined organic extracts were washed with water, saturated aqueous sodium chloride, dried with sodium sulfate, filtered and evaporated. The crude material was purified by reverse phase HPLC (gradient 25-95% acetonitrile in 0.1% aqueous ammonium acetate) to afford the title compound as a white powder. Yield: 21 mg

Workup

  1. stirringThe mixture was stirred at room temperature overnight
  2. stirringThe mixture was shaken vigorously
  3. extractionextracted with ethyl acetate
  4. washThe combined organic extracts were washed with water, saturated aqueous sodium chloride
  5. dry with materialdried with sodium sulfate
  6. filtrationfiltered
  7. customevaporated
  8. customThe crude material was purified by reverse phase HPLC (gradient 25-95% acetonitrile in 0.1% aqueous ammonium acetate)

Sources & evidence

ORD record
ord-fddf989453374f0596b64caabc84bd1e
Source dataset
uspto-grants-2010_11
Patent number
US07838675B2

Reaction notes

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