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1-[Bis-(4-hydroxyphenyl)methyl]-1H-[1,2,4]triazole → 1-[Bis-(3-bromo-4-hydroxyphenyl)methyl]-1H-[1,2,4]triazole

HRID 19960
ノート
印刷プレビュー

反応式

HRID 19960 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:14]2[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=2)[N:9]2[CH:13]=[N:12][CH:11]=[N:10]2)=[CH:4][CH:3]=1.[Br-:21].[Br-:22].[Br-].C([N+](C)(C)C)C1C=CC=CC=1.C([N+](C)(C)C)C1C=CC=CC=1.C([N+](C)(C)C)C1C=CC=CC=1>C(Cl)Cl.CO.O.CCOC(C)=O>[Br:21][C:16]1[CH:15]=[C:14]([CH:8]([C:5]2[CH:6]=[CH:7][C:2]([OH:1])=[C:3]([Br:22])[CH:4]=2)[N:9]2[CH:13]=[N:12][CH:11]=[N:10]2)[CH:19]=[CH:18][C:17]=1[OH:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 219769051-[Bis-(4-hydroxyphenyl)methyl]-1H-[1,2,4]triazoleHCID 53442637Benzyltrimethylammoniumtribromide

生成物 1

HCID 219768921-[Bis-(3-bromo-4-hydroxyphenyl)methyl]-1H-[1,2,4]triazole

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 8857Ethyl Acetate溶媒
HCID 21226129
Dichloromethane methanol
溶媒
2 回

実験手順

To a stirred solution of 1-[Bis-(4-hydroxyphenyl)methyl]-1H-[1,2,4]triazole (STX267, 500 mg, 1.87 mmol) in CH2Cl2/MeOH 1:1 (40 ml) at −78° C. under nitrogen, a solution of benzyltrimethylammonium tribromide (1.49 g, 3.74 mmol) in CH2Cl2/MeOH 1:1 (10 ml) was added dropwise over 45 min. The orange mixture was kept at 0° C. for 7 h and then at room temperature overnight, at which time the solution had become colorless. The reaction mixture was evaporated and the residue that obtained was dissolved in a mixture water (100 mL) and EtOAc (100 mL). The aqueous layer was separated and was further extracted with EtOAc (2×50 mL). The organic extracts were combined and washed with brine, dried (Na2SO4) and evaporated. The crude product was fractionated by flash chromatography (hexane/ethyl acetate, 1:3) and the second fraction that collected gave JRL01105 (STX356) (485 mg) as white solid at about 97% purity; δH (400 MHz, DMSO-d6) 6.90 (1H, s, CH), 6.93 (2H, d, J 8.6 Hz), 7.03 (2H, dd, J 2.1 and 8.6 Hz), 7.30 (2H, d, J 2.1 Hz), 8.06 (1H, s), 8.56 (1H, s) and 10.45 (2H, br s, exchanged with D2O, 2×OH). The main impurity was the mono-brominated derivative of STX356. A small quantity of this fraction was further purified by semi-preparative HPLC (Waters PrepLC RP18, 25×10 mm, flow rate: 10 mL/min, mobile phase: MeOH/H2O, 60:40). The fraction with a retention time of 5.5 nm in was collected and upon evaporation gave a white solid; m.p. 198-205° C. (dec.). Found: C, 42.2; H, 2.65; N, 9.79; C15H11Br2N3O2 requires C, 42.38, H, 2.61, N, 9.89.

後処理

  1. customat room temperature
  2. customovernight
  3. customThe reaction mixture was evaporated
  4. customthe residue that obtained
  5. customThe aqueous layer was separated
  6. extractionwas further extracted with EtOAc (2×50 mL)
  7. washwashed with brine
  8. dry with materialdried (Na2SO4)
  9. customevaporated
  10. customthe second fraction that collected
  11. customgave JRL01105 (STX356) (485 mg) as white solid at about 97% purity
  12. customA small quantity of this fraction was further purified by semi-preparative HPLC (Waters PrepLC RP18, 25×10 mm, flow rate: 10 mL/min, mobile phase: MeOH/H2O, 60:40)
  13. customThe fraction with a retention time of 5.5 nm in was collected and upon evaporation
  14. customgave a white solid

出典と根拠

ORDレコード
ord-51e4072d137f4ce39b82538f57875854
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07745472B2

反応ノート

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