Pyridine → 7-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carbonyl chloride

HRID 473849

反応式

HRID 473849 の反応式
Cl.[Br:2][C:3]1[CH:4]=[CH:5][C:6]2[O:12][CH2:11][CH2:10][NH:9][CH2:8][C:7]=2[CH:13]=1.CCN(C(C)C)C(C)C.N1C=CC=CC=1.[C:29](Cl)([Cl:31])=[O:30]>ClCCl>[Br:2][C:3]1[CH:4]=[CH:5][C:6]2[O:12][CH2:11][CH2:10][N:9]([C:29]([Cl:31])=[O:30])[CH2:8][C:7]=2[CH:13]=1

参加物

6

実験手順

7-bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride (3.0 g, 11.34 mmol) was suspended in dichloromethane (30 mL) followed by addition of DIPEA (3 mL, 34 mmol) and pyridine (4 mL, 49 mmol) and the resulting partially heterogeneous mixture was added portionwise over 5 minutes to a 0° C. cooled solution of phosgene (20 W % in toluene, 15 mL, 28 mmol) in dichloromethane (15 mL). The resulting mixture was then allowed to slowly warm to room temperature over 30 minutes then concentrated. The residue was partitioned with ethyl acetate and water and the organic phase washed twice with 1M aqueous hydrochloric acid then brine, dried over anhydrous magnesium sulfate, filtered and concentrated to give 7-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carbonyl chloride (3.35 g) as a pale yellow oil. MS (EI) for C10H9BrClNO2: 292 (MH+).

後処理

  1. additionthe resulting partially heterogeneous mixture was added portionwise over 5 minutes to a 0° C.
  2. concentrationthen concentrated
  3. customThe residue was partitioned with ethyl acetate and water
  4. washthe organic phase washed twice with 1M aqueous hydrochloric acid
  5. dry with materialbrine, dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-28ce653894fe44dab97a9617993ac516
出典データセット
uspto-grants-2014_01
特許番号
US08637499B2

関連ノート

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