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Potassium Phosphate, Tribasic → 5-[3-(6-Bromo-1-methyl-1H-indazol-3-ylamino)-phenyl]-5-methyl-morpholin-3-one

HRID 925442
ノート
印刷プレビュー

反応式

HRID 925442 の反応式
Br[C:2]1[CH:3]=[C:4]([C:8]2([CH3:15])[NH:13][C:12](=[O:14])[CH2:11][O:10][CH2:9]2)[CH:5]=[CH:6][CH:7]=1.[Br:16][C:17]1[CH:25]=[C:24]2[C:20]([C:21]([NH2:27])=[N:22][N:23]2[CH3:26])=[CH:19][CH:18]=1.CC(C1C=C(C(C)C)C(C2C=CC=CC=2P(C2CCCCC2)C2CCCCC2)=C(C(C)C)C=1)C.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>C1(C)C=CC=CC=1.O.C([O-])(O)=O.[Na+].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.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].CCOC(C)=O>[Br:16][C:17]1[CH:25]=[C:24]2[C:20]([C:21]([NH:27][C:2]3[CH:3]=[C:4]([C:8]4([CH3:15])[NH:13][C:12](=[O:14])[CH2:11][O:10][CH2:9]4)[CH:5]=[CH:6][CH:7]=3)=[N:22][N:23]2[CH3:26])=[CH:19][CH:18]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

10

反応物 4

HCID 62657Potassium Phosphate, TribasicHCID 111557942-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 468355496-Bromo-1-methyl-1H-indazol-3-amineHCID 581553055-(3-Bromophenyl)-5-methylmorpholin-3-one

生成物 1

HCID 895001935-[3-(6-Bromo-1-methyl-1H-indazol-3-ylamino)-phenyl]-5-methyl-morpholin-3-one

試薬・触媒・溶媒 5

HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 962Water溶媒2 回
HCID 1140Toluene溶媒
HCID 8857Ethyl Acetate溶媒
HCID 516892Sodium Bicarbonate溶媒

反応条件

温度
120 °C

実験手順

A mixture of 5-(3-bromo-phenyl)-5-methyl-morpholin-3-one [Example 1, step f)] (CAS registry 1262858-67-2) (138.5 mg, 0.513 mmol), 6-bromo-1-methyl-1H-indazol-3-ylamine (CAS registry 1214899-85-0) (116 mg, 0.513 mmol), X-phos (78 mg, 0.164 mmol) and K3PO4 (218 mg, 1.025 mmol) in toluene (2.5 ml) and water (0.250 ml) was degassed with argon (5 min), then Pd2(dba)3 (37.6 mg, 0.041 mmol) was added and the reaction mixture was stirred at 120° C. for 20 h. The reaction mixture was diluted with water, sat. aq. NaHCO3 soln. and EtOAc. The layers were separated and the aq. layer was twice reextracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The resulting crude product was purified by RP-HPLC (Waters SunFire C18 column, 5 μM, 19×150 mm, gradient 10 to 70% ACN+0.1% TFA) to yield the title compound as a pale yellow powder.

後処理

  1. customwas degassed with argon (5 min)
  2. customThe layers were separated
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe resulting crude product was purified by RP-HPLC (Waters SunFire C18 column, 5 μM, 19×150 mm, gradient 10 to 70% ACN+0.1% TFA)

出典と根拠

ORDレコード
ord-7dc8aa5297e74ee299e2b9d0d522908f
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09284284B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート