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1,2-Dibromoethane → HCID 66920426, 화합물

HRID 1510082
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HRID 1510082 반응식
BrCCBr.[F:5][C:6]1[C:7]([CH3:14])=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH2:9]Br.[C:15]([O:19][C:20]([N:22]1[CH2:27][CH2:26][N:25]([C:28]([C:30]2[C:38]3[C:33](=[CH:34][CH:35]=[C:36]([O:39][CH3:40])[CH:37]=3)[N:32]([C:41]3[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=3)[C:31]=2Cl)=[O:29])[CH2:24][CH2:23]1)=[O:21])([CH3:18])([CH3:17])[CH3:16].COC1C=CC=C(OC)C=1C1C=CC=CC=1P(C1CCCCC1)C1CCCCC1>C1COCC1.[Zn].C([O-])(=O)C.[Pd+2].C([O-])(=O)C.CN(C=O)C>[C:15]([O:19][C:20]([N:22]1[CH2:27][CH2:26][N:25]([C:28]([C:30]2[C:38]3[C:33](=[CH:34][CH:35]=[C:36]([O:39][CH3:40])[CH:37]=3)[N:32]([C:41]3[CH:42]=[CH:43][CH:44]=[CH:45][CH:46]=3)[C:31]=2[CH2:9][C:8]2[CH:11]=[CH:12][CH:13]=[C:6]([F:5])[C:7]=2[CH3:14])=[O:29])[CH2:24][CH2:23]1)=[O:21])([CH3:18])([CH3:16])[CH3:17]
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참가 물질

9

반응물 4

HCID 78391,2-DibromoethaneHCID 27792443-Fluoro-2-methylbenzyl bromideHCID 112698722-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 669202494-(2-Chloro-5-methoxy-1-phenyl-1h-indole-3-carbonyl)-piperazine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 66920426HCID 66920426, 화합물수율 52.7%

시약·촉매·용매 4

HCID 23994Zinc촉매HCID 167845palladium(II) acetate촉매HCID 6228Dimethylformamide용매HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

To a suspension of zinc (322 mg, 4.92 mmol) in dry THF (770 μl) in a dry flask under argon was added 1,2-dibromoethane (10.6 μl, 0.123 mmol). The mixture was heated three times to reflux with a heat-gun. After 5 min the flask was placed in an ice bath and a solution of 3-fluoro-2-methyl-benzylbromide (500 mg, 2.46 mmol) in dry THF (1.5 ml) was added slowly, so that the temperature remained at 0° C. The mixture was stirred at 0° C. for 3 h. The cooled suspension was added dropwise to a precooled solution (−78° C.) of B-OM-9-BBN (2.45 ml, 2.45 mmol, 1 M in hexane). The mixture was then stirred at room temperature for 30 min. DMF (7 ml) was added, followed by the compound of step 5 (115 mg, 245 μmol), palladium(II) acetate (5.49 mg, 24.5 μmol) and S—PHOS (20.1 mg, 48.9 μmol). The reaction mixture was stirred at 100° C. for 2 h. The cooled mixture was quenched with water and extracted with EA. The organic layer was separated, dried over sodium sulfate, filtered, and evaporated under reduced pressure. The residue was purified by preparative HPLC. The eluate was lyophilized overnight to give 72 mg of the title compound.

후처리

  1. temperatureThe mixture was heated three times
  2. temperatureto reflux with a heat-gun
  3. customremained at 0° C
  4. stirringThe mixture was then stirred at room temperature for 30 min
  5. stirringThe reaction mixture was stirred at 100° C. for 2 h
  6. customThe cooled mixture was quenched with water
  7. extractionextracted with EA
  8. customThe organic layer was separated
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. customevaporated under reduced pressure
  12. customThe residue was purified by preparative HPLC
  13. waitThe eluate was lyophilized overnight

출처 및 근거

ORD 기록
ord-83f15201a9c143498f83c2c84e50f1b5
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211885B2

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