Cesium carbonate → 2-Bromo-6-(8-tert-butyl-5-oxo-1,2,3,5-tetrahydrobenzo[e][1,4]diazepin-4-yl)-benzaldehyde

HRID 1879673

反応式

HRID 1879673 の反応式
[C:1]([C:5]1[CH:6]=[CH:7][C:8]2[C:14](=[O:15])[NH:13][CH2:12][CH2:11][NH:10][C:9]=2[CH:16]=1)([CH3:4])([CH3:3])[CH3:2].[Br:17][C:18]1[CH:25]=[CH:24][CH:23]=[C:22](Br)[C:19]=1[CH:20]=[O:21].CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2.C(=O)([O-])[O-].[Cs+].[Cs+]>O1CCOCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd]>[Br:17][C:18]1[CH:25]=[CH:24][CH:23]=[C:22]([N:13]2[C:14](=[O:15])[C:8]3[CH:7]=[CH:6][C:5]([C:1]([CH3:4])([CH3:2])[CH3:3])=[CH:16][C:9]=3[NH:10][CH2:11][CH2:12]2)[C:19]=1[CH:20]=[O:21]

参加物

7

反応物 4

HCID 10796Cesium carbonateHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 126486412,6-DibromobenzaldehydeHCID 595485328-tert-Butyl-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one

生成物 1

HCID 595485362-Bromo-6-(8-tert-butyl-5-oxo-1,2,3,5-tetrahydrobenzo[e][1,4]diazepin-4-yl)-benzaldehyde

試薬・触媒・溶媒 2

HCID 6505921(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium触媒HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
100 °C

実験手順

8-tert-Butyl-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one (420 mg, 2 mmol), 2,6-Dibromo-benzaldehyde (2.03 g, 8 mmol, 3eq), Xanthphos (22 mg, 0.02eq), and cesium carbonate (1.23 g, 4 mmol, 2 eq) were taken up in dioxane (5.0 mL) and a stream of argon gas was bubbled through the mixture for 1 minute. The catalyst Pd(dba)2 (33 mg, 0.03 eq) was added and argon was bubbled through for an additional minute. The resulting mixture was sealed under argon and stirred at 100° C. for 18 hours. The reaction was cooled and filtered. The collected solid was triturated with water and filtered to give a solid. The dioxane filtrate was combined with this solid, the solvent removed under vacuum, and the residue chromatographed, eluting with 50% ethyl acetate in hexanes gave a solid, 81 mg. (M+H)+=402.

後処理

  1. customa stream of argon gas was bubbled through the mixture for 1 minute
  2. customargon was bubbled through for an additional minute
  3. customThe resulting mixture was sealed under argon
  4. temperatureThe reaction was cooled
  5. filtrationfiltered
  6. customThe collected solid was triturated with water
  7. filtrationfiltered
  8. customto give a solid
  9. customthe solvent removed under vacuum
  10. customthe residue chromatographed
  11. washeluting with 50% ethyl acetate in hexanes
  12. customgave a solid, 81 mg

出典と根拠

ORDレコード
ord-ed7acf2dedb64cccaed3e5bd00607747
出典データセット
uspto-grants-2012_11
特許番号
US08318719B2

関連ノート

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