Iodine → Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl ester

HRID 16053

반응식

HRID 16053 반응식
N(OCCC(C)C)=O.[C:9]([O:12][CH2:13][C@@H:14]1[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@@H:17]([O:23][C:24](=[O:26])[CH3:25])[C@H:16]([N:27]2[CH:35]=[N:34][C:33]3[C:28]2=[N:29][C:30](N)=[N:31][C:32]=3[Cl:36])[O:15]1)(=[O:11])[CH3:10].II.C(I)[I:41].[O-]S([O-])(=S)=O.[Na+].[Na+]>C1COCC1.[Cu]I>[C:9]([O:12][CH2:13][C@@H:14]1[C@@H:18]([O:19][C:20](=[O:22])[CH3:21])[C@@H:17]([O:23][C:24](=[O:26])[CH3:25])[C@H:16]([N:27]2[CH:35]=[N:34][C:33]3[C:28]2=[N:29][C:30]([I:41])=[N:31][C:32]=3[Cl:36])[O:15]1)(=[O:11])[CH3:10]

참가 물질

8

반응물 5

HCID 807IodineHCID 6346DiiodomethaneHCID 8053Isoamyl NitriteHCID 24477Sodium ThiosulfateHCID 10788628(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(2-amino-6-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate

생성물 1

HCID 482588Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl ester

시약·촉매·용매 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 8028Tetrahydrofuran용매

실험 절차

Isoamyl nitrite (5 mL, 37 mmol) was added to a mixture of 5.12 g (12 mmol) [(2R,3R,4R,5R)-3-,4-diacetyloxy-5-(2-amino-6-chloropurin-9-yl)oxolan-2-yl]methy 1 acetate (6.3), I2 (3.04 g, 12 mmol), CH2I2 (10 mL, 124 mmol), and CuI (2.4 g, 12.6 mmol) in THF (60 mL). The mixture was heated under reflux for 45 minutes and then allowed to cool to room temperature. To this solution was added 100 ml of saturated Na2S2O3. This step removed the reddish color. The aqueous layer was extracted 3× with chloroform, which was pooled, dried over MgSO4, and concentrated under reduced pressure. The product was then purified over a silica gel column using CHCl3-MeOH (98:2) to collect [(2R,3R,4R,5R)-3,4-diacetyloxy-5-(6-chloro-2-iodopurin-9-yl)oxolan-2-yl]methyl acetate (6.4) (80% crystallized from EtOH). 1H NMR (300 MHz, CDCl3) 8.20 (s, 1H H-8), 6.17 (d, J=5.41 Hz, 1H, H-1), 5.75 (t, J=5.39 Hz, 1H, H-2), 5.56 (t, J=5.40 Hz, 1H, 1H-3), 4.38 (m, 3H, 1H-4,5), 2.14 (s, 1H, Ac), 2.11 (s, 1H, Ac), 2.10 (s, 1H, Ac).

후처리

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 45 minutes
  3. customThis step removed the reddish color
  4. extractionThe aqueous layer was extracted 3× with chloroform, which
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated under reduced pressure
  7. customThe product was then purified over a silica gel column
  8. customto collect [(2R,3R,4R,5R)-3,4-diacetyloxy-5-(6-chloro-2-iodopurin-9-yl)oxolan-2-yl]methyl acetate (6.4) (80% crystallized from EtOH)

출처 및 근거

ORD 기록
ord-010ac816cca847b6816acb77f5c7b247
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07737127B2

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