Hydrochloric Acid → Hydrochloric Acid

HRID 2366576Notes

Reaction equation

HRID 2366576 reaction equation
[F:1][C:2]([F:23])([F:22])[O:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[O:19][CH2:18][CH2:17][NH:16][C:15](=O)[C:14]=3[CH:21]=2)=[CH:6][CH:5]=1.CO.[ClH:26]>C1COCC1.B>[F:23][C:2]([F:1])([F:22])[O:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[O:19][CH2:18][CH2:17][NH:16][CH2:15][C:14]=3[CH:21]=2)=[CH:6][CH:5]=1.[ClH:26]

Participants

7

Conditions

Temperature
70 °C

Procedure

To a solution of 7-(4-(trifluoromethoxy)phenyl)-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one (660 mgs, 2.0 mmol) in THF (6 mL), 1.0M Borane in THF (6.0 mL, 6.0 mmol) was added and the mixture was heated at 70° C. After 16 h, the mixture was cooled to rt and Methanol (22 mL) and 6.0M HCl (22 mL) was added and stirred at rt for 2 h. The reaction mixture was then concentrated and the solids formed were filtered and washed with ether and dried to give 7-(4-(trifluoromethoxy)phenyl)-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepine as HCl salt. The above compound (100 mgs, 0.29 mmol), pyrimidine-2-carboxylic acid (47 mgs, 0.38 mmol), HATU (143 mgs, 0.38 mmol), in DMF (1 mL) was added NMM (0.1 mL, 0.86 mmol) and stirred at 60° C. for 30 min. The reaction mixture was then diluted with EtOAc and washed with NaHCO3, brine and dried (MgS(O)4). The mixture was the filtered, concentrated and chromatographed (SiO2, 50% EtOAc/DCM) to provide the title compound.

Workup

  1. temperaturethe mixture was cooled to rt
  2. concentrationThe reaction mixture was then concentrated
  3. customthe solids formed
  4. filtrationwere filtered
  5. washwashed with ether
  6. customdried

Sources & evidence

ORD record
ord-f1086e06719042d7a17316e1244d0eda
Source dataset
uspto-grants-2014_04
Patent number
US08697863B2

Reaction notes

Loading…