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Tri-o-tolylphosphine → HCID 178418607、化合物

HRID 6529
ノート
印刷プレビュー

反応式

HRID 6529 の反応式
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][CH:9]=[CH:10][N:11]1[C:16]([OH:17])=[C:15]2[CH:18]=[C:19]([NH:21][C:22](=[O:27])[C:23]([CH3:26])([CH3:25])[CH3:24])[N:20]=[C:14]2[N:13]=[CH:12]1.I[C:29]1[CH:50]=[CH:49][C:32]([C:33]([NH:35][C@H:36]([C:44]([O:46][CH2:47][CH3:48])=[O:45])[CH2:37][CH2:38][C:39]([O:41][CH2:42][CH3:43])=[O:40])=[O:34])=[CH:31][CH:30]=1.CC1C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.IC1C=CC(C(N[C@H](C(OCC)=O)CCC([O-])=O)=O)=CC=1>C(N(CC)CC)C.C(#N)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][C:9]([C:29]1[CH:50]=[CH:49][C:32]([C:33]([NH:35][C@H:36]([C:44]([O:46][CH2:47][CH3:48])=[O:45])[CH2:37][CH2:38][C:39]([O:41][CH2:42][CH3:43])=[O:40])=[O:34])=[CH:31][CH:30]=1)=[CH:10][N:11]1[C:16]([OH:17])=[C:15]2[CH:18]=[C:19]([NH:21][C:22](=[O:27])[C:23]([CH3:24])([CH3:26])[CH3:25])[N:20]=[C:14]2[N:13]=[CH:12]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 80271Tri-o-tolylphosphineHCID 1885228diethyl (2S)-2-[(4-iodobenzoyl)amino]pentanedioateHCID 86747251ethyl N-(4-iodobenzoyl)glutamateHCID 178418674HCID 178418674、化合物

生成物 1

HCID 178418607HCID 178418607、化合物

試薬・触媒・溶媒 3

HCID 167845
palladium(II) acetate
触媒
HCID 6342Acetonitrile溶媒
HCID 8471Triethylamine溶媒

実験手順

A mixture containing 3.48 g of 3-(3-tetrahydropyr-2-yloxyprop-1-en-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 3.12g (1.2 equiv.) of diethyl N-(4-iodobenzoyl)glutamate, 546 mg (20%) of tris-(2-methylphenyl)phosphine, 201 mg (10%) of palladium acetate and 85.5 mg (5%) of cuprous iodide in 15 ml of triethylamine and 240 ml of acetonitrile is heated at reflux under nitrogen. After 12 hours., 1.17 g of ethyl N-(4-iodobenzoyl)glutamate are added and the reaction mixture is heated at reflux under nitrogen for an additional 12 hours. The reaction mixture then is concentrated under reduced pressure and the residue chromatographed on silica gel, eluting with 20:1 ethyl acetate:hexane. (Any recovered starting material can be recycled through the foregoing procedure.) The concentrated material is dissolved in 1:5 ethyl acetate:ether and this solution is refrigerated for 15 hours. The solid which forms is collected by filtration, washed with cold ethyl acetate and dried to yield diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate.

後処理

  1. temperatureis heated
  2. temperatureat reflux under nitrogen
  3. temperaturethe reaction mixture is heated
  4. temperatureat reflux under nitrogen for an additional 12 hours
  5. concentrationThe reaction mixture then is concentrated under reduced pressure
  6. customthe residue chromatographed on silica gel
  7. washeluting with 20:1 ethyl acetate
  8. dissolution) The concentrated material is dissolved in 1:5 ethyl acetate
  9. waitether and this solution is refrigerated for 15 hours
  10. filtrationThe solid which forms is collected by filtration
  11. washwashed with cold ethyl acetate
  12. customdried

出典と根拠

ORDレコード
ord-f4b94ff8ba9e4c06ac8d51b313e46253
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05248775

反応ノート

読み込み中…

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