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Dichloromethane → HCID 86700204、化合物

HRID 879397
ノート
印刷プレビュー

反応式

HRID 879397 の反応式
Cl[C:2]1[CH:3]=[C:4]([C:8]2[CH:9]=[C:10]3[C:14](=[CH:15][CH:16]=2)[N:13]([CH3:17])[N:12]=[CH:11]3)[N:5]=[N:6][CH:7]=1.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.ClCCl.C([O-])(=O)C.[K+].Br[C:45]1[S:46][C:47]2[C:53]([C:54]3[CH:59]=[CH:58][C:57]([Cl:60])=[CH:56][CH:55]=3)=[C:52]([C@H:61]([O:67][C:68]([CH3:71])([CH3:70])[CH3:69])[C:62]([O:64][CH2:65][CH3:66])=[O:63])[C:51]([CH3:72])=[CH:50][C:48]=2[N:49]=1.C([O-])([O-])=O.[K+].[K+]>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:68]([O:67][C@@H:61]([C:52]1[C:51]([CH3:72])=[CH:50][C:48]2[N:49]=[C:45]([C:2]3[CH:3]=[C:4]([C:8]4[CH:9]=[C:10]5[C:14](=[CH:15][CH:16]=4)[N:13]([CH3:17])[N:12]=[CH:11]5)[N:5]=[N:6][CH:7]=3)[S:46][C:47]=2[C:53]=1[C:54]1[CH:55]=[CH:56][C:57]([Cl:60])=[CH:58][CH:59]=1)[C:62]([O:64][CH2:65][CH3:66])=[O:63])([CH3:69])([CH3:70])[CH3:71]
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

8

反応物 6

HCID 6344DichloromethaneHCID 11430Potassium CarbonateHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 86700141(S)-ethyl 2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetateHCID 867002035-(5-chloropyridazin-3-yl)-1-methyl-1H-indazole

生成物 1

HCID 86700204HCID 86700204、化合物

試薬・触媒・溶媒 1

HCID 178418397HCID 178418397、化合物触媒

反応条件

温度
110 °C

実験手順

5-(5-chloropyridazin-3-yl)-1-methyl-1H-indazole (75.0 mg, 0.307 mmol), bis(pinacolato)diboron (101.2 mg, 0.398 mmol), [1,1′Bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (37.5 mg, 0.046 mmol), and potassium acetate (90.2 mg, 0.920 mmol) were taken in a microwave vial, and the vial was vacuum pumped and flushed with argon three times. To this mixture was added degassed DMF (3 mL). The reaction mixture was heated at 110° C. for 2 h then cooled. To the cooled reaction mixture was added (S)-ethyl 2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetate (180.0 mg, 0.368 mmol), tetrakis(triphenylphosphine)palladium(0) (53.1 mg, 0.046 mmol), K2CO3 (127.1 mg, 0.920 mmol) and degassed water (0.5 mL). The reaction mixture was heated to 110° C. for 2 h, cooled, filtered through Celite (ethyl acetate eluent), and concentrated. Purification by flash column chromatography on silica gel (hexanes/ethyl acetate eluent) provided the product. LCMS-ESI+ calc'd for C34H33ClN5O3S (M+H+): 626.2; Found: 625.5 (M+H+).

後処理

  1. customflushed with argon three times
  2. additionTo this mixture was added
  3. customdegassed DMF (3 mL)
  4. temperaturethen cooled
  5. customTo the cooled reaction mixture
  6. customdegassed water (0.5 mL)
  7. temperatureThe reaction mixture was heated to 110° C. for 2 h
  8. temperaturecooled
  9. filtrationfiltered through Celite (ethyl acetate eluent)
  10. concentrationconcentrated
  11. customPurification by flash column chromatography on silica gel (hexanes/ethyl acetate eluent)
  12. customprovided the product

出典と根拠

ORDレコード
ord-e9012eb478414b22ab142c8b44f47236
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987250B2

反応ノート

読み込み中…

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