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Hydrochloric Acid → 2-Amino-9-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)adenine

HRID 1448995
ノート
印刷プレビュー

反応式

HRID 1448995 の反応式
Cl.[CH2:2]([O:9][C@H:10]1[C@H:26]([O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C@@H:25]([CH2:35][O:36][CH2:37][C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)[O:24][C@H:11]1OC(=O)C1C=CC([N+]([O-])=O)=CC=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C([NH:47][C:48]1[N:56]=[C:55]2[C:51]([NH:52][CH:53]=[N:54]2)=[C:50]([NH:57]C(=O)C)[N:49]=1)(=O)C>C(Cl)Cl.C(Cl)CCl>[NH2:47][C:48]1[N:56]=[C:55]2[C:51]([N:52]=[CH:53][N:54]2[C@@H:11]2[O:24][C@H:25]([CH2:35][O:36][CH2:37][C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)[C@@H:26]([O:27][CH2:28][C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[C@@H:10]2[O:9][CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)=[C:50]([NH2:57])[N:49]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 71572112,3,5-tri-O-benzyl-1-O-p-nitrobenzoyl-beta-D-arabinofuranoseHCID 13923314N,N'-(7H-Purine-2,6-diyl)diacetamide

生成物 1

HCID 108969412-Amino-9-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)adenine

試薬・触媒・溶媒 2

HCID 111,2-Dichloroethane溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

Dry HCl gas was bubbled into a solution of 2,3,5-tri-O-benzyl-1-O-p-nitrobenzoyl-β-D-arabinofuranose (17 g, 30 mmol) in CH2Cl2 (187 ml) at -10°-0° for 21/2 hr. The precipitated p-nitrobenzoic acid was removed by filtration and washed with CH2Cl2. The CH2Cl2 solution was evaporated in vacuo. The residue, dissolved in 500 ml of ethylene chloride, was added to a mixture of 2.6-diacetamidopurine (7.03 g, 30 mmol) and molecular sieve (Linde 4A, 75 g) in 500 ml of ethylene chloride. This mixture was refluxed until all the chlorosugar was consumed (TLC) (8-11 days). The mixture was then stirred with Celite and filtered. The solid was washed with CHCl3, and the combined filtrates were evaporated to dryness in vacuo. The residue was dissolved in benzene and filtered (to remove unreacted 2,6-diacetamidopurine). The filtrate was again evaporated to dryness in vacuo and the residue dissolved in 100 ml of 1 N methanolic NaOMe. After a 3-hr reflux period, the solution was chilled, neutralized with acetic acid, and refrigerated overnight. The solid that precipitated was removed by filtration, washed with MeOH, and dried in vacuo; yield 5.6 g (34%); mp 159°-161°; TLC homogenous.

後処理

  1. customThe precipitated p-nitrobenzoic acid was removed by filtration
  2. washwashed with CH2Cl2
  3. customThe CH2Cl2 solution was evaporated in vacuo
  4. dissolutionThe residue, dissolved in 500 ml of ethylene chloride
  5. temperatureThis mixture was refluxed until all the chlorosugar
  6. customwas consumed (TLC) (8-11 days)
  7. filtrationfiltered
  8. washThe solid was washed with CHCl3
  9. customthe combined filtrates were evaporated to dryness in vacuo
  10. dissolutionThe residue was dissolved in benzene
  11. filtrationfiltered
  12. custom(to remove unreacted 2,6-diacetamidopurine)
  13. customThe filtrate was again evaporated to dryness in vacuo
  14. dissolutionthe residue dissolved in 100 ml of 1 N methanolic NaOMe
  15. temperatureAfter a 3-hr reflux period
  16. temperaturethe solution was chilled
  17. customneutralized with acetic acid, and refrigerated overnight
  18. customThe solid that precipitated
  19. customwas removed by filtration
  20. washwashed with MeOH
  21. customdried in vacuo

出典と根拠

ORDレコード
ord-2d1a9d7b5af74b2ba1e69f2f23f8f45d
出典データセット
uspto-grants-1980_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04188378

反応ノート

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