Bromomethylcyclopropane → HCID 67215162, compound

HRID 1983100Notes

Reaction equation

HRID 1983100 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH2:26])[CH:6]=[CH:7][C:8]=1[C:9]1[O:10][C:11]([C:14]2[C:15]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[N:16][O:17][C:18]=2[CH3:19])=[N:12][N:13]=1.C(N(CC)C(C)C)(C)C.Br[CH2:37][CH:38]1[CH2:40][CH2:39]1.C[Si]([N-][Si](C)(C)C)(C)C.[K+]>C1COCC1>[CH:38]1([CH2:37][CH2:19][C:18]2[O:17][N:16]=[C:15]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[C:14]=2[C:11]2[O:10][C:9]([C:8]3[CH:7]=[CH:6][C:5]([NH2:26])=[CH:4][C:3]=3[O:2][CH3:1])=[N:13][N:12]=2)[CH2:40][CH2:39]1

Participants

6

Reactant 4

HCID 81503Bromomethylcyclopropane3×HCID 81531DiisopropylethylamineHCID 3251421Potassium bis(trimethylsilyl)amideHCID 167225873-Methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenylamine

Product 1

HCID 67215162HCID 67215162, compoundYield 12.2%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a suspension of 3-methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenylamine (200 mg, 0.57 mmol) in THF were added N,N-diisopropyl ethyl amine (128 μL, 0.75 mmol) and bromomethyl-cyclopropane (61 μL, 0.63 mmol) and the reaction mixture was stirred for 24 h at ambient temperature. After addition of potassium bis(trimethylsilyl)amide (0.91 M in THF, 0.82 mL, 0.75 mmol) was added stirring was continued for 15 min and further bromomethyl-cyclopropane (78 μL, 0.80 mmol) was added. After stirring for 18 h at ambient temperature further bromomethyl-cyclopropane (0.12 mL, 1.2 mmol) was added and stirring continued for 24 h at this temperature. The reaction mixture was extracted with aqueous sodium carbonate (saturated, 20 mL) and ethyl acetate (20 mL). The aqueous layer was extracted with ethyl acetate (20 mL) and the combined organic layers dried over sodium sulfate. Concentration and then purification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane=40:40:20 to 0:80:20) afforded the title compound (28 mg, 12%) as a light brown solid. MS: m/e=403.4 [M+H]+.

Workup

  1. additionwas added
  2. stirringstirring
  3. waitwas continued for 15 min
  4. additionwas added
  5. stirringstirring
  6. waitcontinued for 24 h at this temperature
  7. extractionThe reaction mixture was extracted with aqueous sodium carbonate (saturated, 20 mL) and ethyl acetate (20 mL)
  8. extractionThe aqueous layer was extracted with ethyl acetate (20 mL)
  9. dry with materialthe combined organic layers dried over sodium sulfate
  10. concentrationConcentration
  11. custompurification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane=40:40:20 to 0:80:20)

Sources & evidence

ORD record
ord-140030926a79409ea4f3757b35c8de26
Source dataset
uspto-grants-2009_06
Patent number
US07541372B2

Reaction notes

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