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Oxygen → Carboprost tromethamine

HRID 437893
ノート
印刷プレビュー

反応式

HRID 437893 の反応式
[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][C@:6]([OH:26])(/[CH:8]=[CH:9]/[C@@H:10]1[C@@H:14]([CH2:15]/[CH:16]=[CH:17]/[CH2:18][CH2:19][CH2:20][C:21]([OH:23])=[O:22])[C@@H:13]([OH:24])[CH2:12][C@H:11]1[OH:25])[CH3:7].O=O.C1C=C(SSC2N=CC=CC=2)N=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(OCC)(=O)C.CCOC(C)=O.CCCCCC.C1(C)C(C)=CC=CC=1>[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][C@:6]([OH:26])(/[CH:8]=[CH:9]/[C@@H:10]1[C@@H:14]([CH2:15]/[CH:16]=[CH:17]\[CH2:18][CH2:19][CH2:20][C:21]([OH:23])=[O:22])[C@@H:13]([OH:24])[CH2:12][C@@H:11]1[OH:25])[CH3:7]
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 977OxygenHCID 11776TriphenylphosphineHCID 650932,2'-Dipyridyl disulfideHCID 5284525(E)-7-((1R,2R,3R,5S)-3,5-Dihydroxy-2-((E)-(3S)-3-hydroxy-3-methyloct-1-enyl)cyclopentyl)-5-heptenoic acid

生成物 1

HCID 35023177Carboprost tromethamine

試薬・触媒・溶媒 3

HCID 7237
O-Xylene
溶媒
HCID 8857Ethyl Acetate溶媒
HCID 21226206Ethyl acetate hexane溶媒

実験手順

A solution of 15-methyl-PGF2α (185 mg.) in 2.5 ml. of an anhydrous, oxygen-free xylene containing 2,2'-dipyridyl disulfide (165 mg.) and triphenylphosphine (196 mg.) is stirred under nitrogen for 2.5 hr. at 25° C. The mixture is diluted with 150 ml. of xylene and heated at reflux for 3 hr. TLC (80 percent EtOAc/hexane) shows essentially a single, less polar product. The xylene is removed by evaporation at reduced pressure to afford a residue which is diluted with ice/water/sodium bicarbonate and ethyl acetate and extracted thoroughly with ethyl acetate. The ethyl acetate extract is washed with brine, dried over anhydrous sodium sulfate and concentrated to afford a residue of (15S)-15-methyl PGF2α, 1,9-lactone. The residue is purified by chromatography on 50 g. of neutral silica packed with 10 percent acetone/methylene chloride and eluted (5 ml. fractions) with 200 ml. of 10 percent acetone/methylene chloride, 1500 ml. of 20 percent acetone/methylene chloride and 1000 ml. of 35 percent acetone/methylene chloride.

後処理

  1. customat 25° C
  2. additionThe mixture is diluted with 150 ml
  3. temperatureat reflux for 3 hr
  4. customThe xylene is removed by evaporation at reduced pressure
  5. customto afford a residue which
  6. extractionextracted thoroughly with ethyl acetate
  7. extractionThe ethyl acetate extract
  8. washis washed with brine
  9. dry with materialdried over anhydrous sodium sulfate
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-e0b4d23c2be344eb85ff2488554c9617
出典データセット
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04032543

反応ノート

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