Triethylamine → HCID 178418686、化合物

HRID 2226015

反応式

HRID 2226015 の反応式
I[N:2]1[C:7]([OH:8])=[C:6]2[CH:9]=[C:10]([NH:12][C:13](=[O:18])[C:14]([CH3:17])([CH3:16])[CH3:15])[N:11]=[C:5]2[N:4]=[CH:3]1.[CH3:19][Si:20]([C:23]#[CH:24])([CH3:22])[CH3:21].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)CC)C>C(#N)C.[Pd](Cl)Cl>[CH3:19][Si:20]([C:23]#[C:24][N:2]1[C:7]([OH:8])=[C:6]2[CH:9]=[C:10]([NH:12][C:13](=[O:18])[C:14]([CH3:17])([CH3:16])[CH3:15])[N:11]=[C:5]2[N:4]=[CH:3]1)([CH3:22])[CH3:21]

参加物

7

反応物 4

HCID 8471TriethylamineHCID 11776TriphenylphosphineHCID 66111TrimethylsilylacetyleneHCID 178418587HCID 178418587、化合物

生成物 1

HCID 178418686HCID 178418686、化合物

試薬・触媒・溶媒 2

HCID 24290Palladium Chloride触媒HCID 6342Acetonitrile溶媒

実験手順

A mixture of 2.0 g of 3-iodo-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 1.2 g. of trimethylsilylacetylene, 0.1 g of palladium chloride, 0.23 g of triphenylphosphine, 0.06 g of cuprous iodide, and 2.6 g of triethylamine in 100 mL of acetonitrile is heated in a sealed tube for 1.5 hours at 50° C. and then at reflux for 3 hours. The solvent is removed under reduced pressure and the residue triturated with 1:1 ethyl acetate:hexanes and filtered. The solid thus collected is dissolved in methylene chloride and this solution is passed through a pad of silica gel eluting with 1% methanol on methylene chloride. The eluate is concentrated to yield 3-trimethylsilylethynyl-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine.

後処理

  1. temperatureat reflux for 3 hours
  2. customThe solvent is removed under reduced pressure
  3. customthe residue triturated with 1:1 ethyl acetate
  4. filtrationhexanes and filtered
  5. customThe solid thus collected
  6. dissolutionis dissolved in methylene chloride
  7. concentrationThe eluate is concentrated

出典と根拠

ORDレコード
ord-960f89a0497445acb7510bde5ef1ec4e
出典データセット
uspto-grants-1994_09
特許番号
US05344932

関連ノート

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