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Dichloromethane → 3-(1-perhydro-2H-pyran-2-yl-5-[1-(triphenylmethyl)(1,2,4-triazol-3-yl)]-1H-indazol-3-yl}phenylamine

HRID 1272838
ノート
印刷プレビュー

反応式

HRID 1272838 の反応式
Br[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]3[N:15]=[CH:14][N:13]([C:16]([C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)[N:12]=3)[CH:9]=2)[N:4]([CH:35]2[CH2:40][CH2:39][CH2:38][CH2:37][O:36]2)[N:3]=1.ClCCl.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>COCCOC.NC1C=C(B(O)O)C=CC=1.C1(P(C2C=CC=CC=2)[C-]2C=CC=C2)C=CC=CC=1.[C-]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=C1.[Fe+2]>[O:36]1[CH2:37][CH2:38][CH2:39][CH2:40][CH:35]1[N:4]1[C:5]2[C:10](=[CH:9][C:8]([C:11]3[N:15]=[CH:14][N:13]([C:16]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)[C:29]4[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=4)[N:12]=3)=[CH:7][CH:6]=2)[C:2]([C:7]2[CH:6]=[C:5]([NH2:4])[CH:10]=[CH:9][CH:8]=2)=[N:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 6344DichloromethaneHCID 62657Potassium Phosphate, TribasicHCID 22479811HCID 22479811、化合物

生成物 1

HCID 211011823-(1-perhydro-2H-pyran-2-yl-5-[1-(triphenylmethyl)(1,2,4-triazol-3-yl)]-1H-indazol-3-yl}phenylamine収率 79%

試薬・触媒・溶媒 3

HCID 635956Ferrocene-1,1'-bis-(diphenylphosphine)
触媒
HCID 80711,2-Dimethoxyethane溶媒
HCID 922693-Aminophenylboronic acid溶媒

実験手順

To a solution of 2-{3-bromo-5-[1 (triphenylmethyl)(1,2,4-triazol-3-yl)]-1H-indazolyl}perhydro-2H-pyran (1.0 g, 1.69 mmol) in ethylene glycol dimethyl ether, (20 mL), 3-amino phenyl boronic acid was added as a solid (0.393 g, 2.53 mmol), followed by [1,1′-bis(diphenylphosphino)-ferrocene] complex with dichloromethane (1:1) (0.196 g, 0.169 mmol), and potassium phosphate (1.79 g, 8.45 mmol). The reaction mixture was heated to reflux temperature of the solvent for 12 h. The crude reaction mixture was partitioned between ethyl acetate and water. The organic extracts were dried over Na2SO4. The desired product was isolated as a beige solid after column chromatography purification (SiO2, 25–50% ethyl acetate in hexanes) (0.801 g, 79% yield): ES-MS (m/z) 603 [M+1]+.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux temperature of the solvent for 12 h
  3. customThe crude reaction mixture
  4. customwas partitioned between ethyl acetate and water
  5. dry with materialThe organic extracts were dried over Na2SO4

出典と根拠

ORDレコード
ord-fa8183b0b7f541a7a1c2a0510017bd24
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07208513B2

反応ノート

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