Hydrochloric Acid → HCID 66954362, compound

HRID 2096977Notes

Reaction equation

HRID 2096977 reaction equation
C([Mg]Cl)(C)C.[CH:6]1([NH:9][C:10]2[C:14]3[CH:15]=[CH:16][CH:17]=[C:18](I)[C:13]=3[O:12][N:11]=2)[CH2:8][CH2:7]1.[B:20](OC(C)C)([O:25]C(C)C)[O:21]C(C)C.Cl>O1CCCC1.O>[CH:6]1([NH:9][C:10]2[C:14]3[CH:15]=[CH:16][CH:17]=[C:18]([B:20]([OH:25])[OH:21])[C:13]=3[O:12][N:11]=2)[CH2:8][CH2:7]1

Participants

7

Conditions

Temperature
0 °C

Procedure

Isopropylmagnesium chloride (2.0 M in tetrahydrofuran, 2.83 mL, 5.7 mmol) was added dropwise over 20 minutes to a stirred solution of N-cyclopropyl-7-iodobenzo[d]isoxazol-3-amine (preparation 22 g, 0.50 g, 1.7 mmol) in tetrahydrofuran (10 mL) at −10° C. The mixture was stirred for 1 hour at 0° C. then triisopropyl borate (1.15 mL, 5.0 mmol) was added dropwise over 10 minutes and the mixture was stirred for 1 hour at 0° C. Then, the mixture was warmed to room temperature and stirred overnight. Water was then added, the mixture was cooled by means of an ice-water bath and the pH was adjusted to 1 with 2M aqueous hydrochloric acid. The mixture was extracted with ethyl acetate and the organic layer was washed with brine, dried (MgSO4) and evaporated. The residue was triturated with diethyl ether and the solid was filtered and dried to give the title compound (140 mg, 39%) as a white solid.

Workup

  1. stirringthe mixture was stirred for 1 hour at 0° C
  2. temperatureThen, the mixture was warmed to room temperature
  3. stirringstirred overnight
  4. temperaturethe mixture was cooled by means of an ice-water bath
  5. extractionThe mixture was extracted with ethyl acetate
  6. washthe organic layer was washed with brine
  7. dry with materialdried (MgSO4)
  8. customevaporated
  9. customThe residue was triturated with diethyl ether
  10. filtrationthe solid was filtered
  11. customdried

Sources & evidence

ORD record
ord-adcc930d20634cdbb4a3beffc0a3cee2
Source dataset
uspto-grants-2013_05
Patent number
US08450341B2

Reaction notes

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