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HCID 54539058、化合物 → HCID 131712512、化合物

HRID 848578
ノート
印刷プレビュー

反応式

HRID 848578 の反応式
[CH2:1]([OH:24])[C@@H:2]([OH:23])[C@H:3]([OH:22])[C@H:4]([O:9][C@@H:10]1[O:15][C@H:14]([C:16]([OH:18])=[O:17])[C@@H:13]([OH:19])[C@H:12]([OH:20])[C@H:11]1[OH:21])[C@@H:5]([NH2:8])[CH:6]=[O:7].BrCC([C@H:29]1[CH2:46][CH2:45][C@@:44]2([CH3:47])[C:31](=[CH:32][CH2:33][C@@H:34]3[C@@H:43]2[CH2:42][CH2:41][C@@:39]2([CH3:40])[C@H:35]3[CH2:36][CH2:37][C:38]2=[O:48])[CH2:30]1)=O>CS(C)=O.[Ag]>[CH2:1]([OH:24])[C@@H:2]([OH:23])[C@H:3]([OH:22])[C@H:4]([O:9][C@@H:10]1[O:15][C@H:14]([C:16]([OH:18])=[O:17])[C@@H:13]([OH:19])[C@H:12]([OH:20])[C@H:11]1[OH:21])[C@@H:5]([NH2:8])[CH:6]=[O:7].[CH3:40][C@@:39]12[C:38](=[O:48])[CH2:37][CH2:36][C@H:35]1[C@@H:34]1[CH2:33][CH:32]=[C:31]3[CH2:30][C@@H:29]([OH:7])[CH2:46][CH2:45][C@:44]3([CH3:47])[C@H:43]1[CH2:42][CH2:41]2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 54539058HCID 54539058、化合物HCID 71586761Chondrosine

生成物 1

HCID 131712512HCID 131712512、化合物

試薬・触媒・溶媒 2

HCID 23954Silver触媒HCID 679Dimethyl Sulfoxide溶媒

実験手順

1.133 Grams (0.00245 mole) of silver salt of chondrosine was dissolved in 70 ml of DMSO (dimethylsulfoxide) and 0.84 g of the compound (1) was added to the solution to react them at room temperature for 2 days. After the reaction, AgBr was separated by a centrifugal separation and DMSO was distilled off from the resulting supernatant at 45° to 50° C. under a reduced pressure and then, 70 ml of ethanol was added to the residual solid and a floating insoluble material was separated and a filtrate was concentrated under a reduced pressure and poured into 2 ml of cold water to precipitate the product. The precipitate was dried and washed with ether and dried to obtain 0.36 g of a conjugate of chondrosine-dehydroepiandrosterone having the formula ##STR1##

後処理

  1. customto react them at room temperature for 2 days
  2. customwas separated by a centrifugal separation and DMSO
  3. distillationwas distilled off from the resulting supernatant at 45° to 50° C. under a reduced pressure
  4. addition70 ml of ethanol was added to the residual solid
  5. customa floating insoluble material was separated
  6. concentrationa filtrate was concentrated under a reduced pressure
  7. additionpoured into 2 ml of cold water
  8. customto precipitate the product
  9. customThe precipitate was dried
  10. washwashed with ether
  11. customdried

出典と根拠

ORDレコード
ord-b5b1ab4784fa4907a795a38cb025b728
出典データセット
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04296233

反応ノート

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