Triethylamine → 5-[(Triethylsilyl)ethynyl]-1H-indole

HRID 1479538ノート

反応式

HRID 1479538 の反応式
I[N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3]1.[CH2:11]([Si:13]([CH2:18][CH3:19])([CH2:16][CH3:17])[C:14]#[CH:15])[CH3:12].C(N(CC)CC)C>[Cu]I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CN(C=O)C>[CH2:14]([Si:13]([C:11]#[C:12][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[NH:2][CH:3]=[CH:4]2)([CH2:18][CH3:19])[CH2:16][CH3:17])[CH3:15]

参加物

7

反応条件

温度
60 °C

実験手順

To a scintillation vial was added -iodo-1H-indole (1.1 eq.), triethyl(ethynyl)silane (1 eq.), triethylamine (5 eq.), and anhydrous DMF (0.2 M). Vacuumed and nitrogen flushed for three times. CuI (0.1 eq.) and bis(triphenylphosphine)dichloro-palladium(II) (0.1 eq) were added. The vial was sealed and heated at 60° C. overnight. Upon completion of the reaction as monitored by TLC, the content of the vial was loaded onto a silica gel column pretreated with hexanes. Column was washed with hexanes and diethylether until all eluents containing product were collected. Carefully distill off hexanes and ether using rotary evaporator with minim heating afforded product 5-((triethylsilyl)ethynyl)-1H-indole as colorless oil, which was carried directly on to the next step.

後処理

  1. customVacuumed and nitrogen flushed for three times
  2. customThe vial was sealed
  3. customUpon completion of the reaction
  4. washColumn was washed with hexanes and diethylether until all eluents
  5. additioncontaining product
  6. customwere collected
  7. distillationCarefully distill off
  8. customhexanes and ether using rotary evaporator with minim
  9. temperatureheating

出典と根拠

ORDレコード
ord-5c173ef3a1ec427b87899a11371dec7b
出典データセット
uspto-grants-2016_08
特許番号
US09408907B2

反応ノート

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