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Bromotrimethylsilane → 2,6-Diamino-9-[1-hydroxy-3-(phosphonomethoxy)prop-2-oxy]purine

HRID 345083
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HRID 345083 반응식
[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[O:11][CH:12]([CH2:24][OH:25])[CH2:13][O:14][CH2:15][P:16]([O:21]CC)([O:18]CC)=[O:17])=[C:4]([NH2:26])[N:3]=1.Br[Si](C)(C)C>ClCCl>[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[O:11][CH:12]([CH2:13][O:14][CH2:15][P:16]([OH:21])([OH:18])=[O:17])[CH2:24][OH:25])=[C:4]([NH2:26])[N:3]=1
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참가 물질

4

반응물 2

HCID 76113BromotrimethylsilaneHCID 199935472,6-Diamino-9-[1-(diethoxyphosphorylmethoxy)-3-hydroxyprop-2-oxy]purine

생성물 1

HCID 199934952,6-Diamino-9-[1-hydroxy-3-(phosphonomethoxy)prop-2-oxy]purine수율 65%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
20 °C

실험 절차

To a solution of 2,6-diamino-9-[1-(diethoxyphosphorylmethoxy)-3-hydroxyprop-2-oxy]purine (100 mg, 0.26 mmol) in dichloromethane, was added bromotrimethylsilane (0.34 ml, 2.6 mmol) and the solution stirred under nitrogen for 4 h at 20° C. The solution was evaporated in vacuo and co-distilled with methanol and toluene. Recrystallisation of the residue with ethanol-water afforded 2,6-diamino-9-[1-hydroxy-3-(phosphonomethoxy)prop-2-oxy]purine (55 mg, 65%) as a white solid m.p. >300° C. decomp. λmax (H2O), 280 (ε10,100), 255 (ε8,400), 212 (ε26,100); νmax (KBr) 3360, 1700, 1660 and 1410 cm-1 ; δH (D2O+NH3) 3.55 (2H, m, CH2OH), 3.89 (4H, m, CH2OCH2P), 4.62 (1H, m, CHON), 8.10 (1 H, s, H-8). Found: C, 32.49; H, 4.63; N, 24.86%; C9H15N6O6P requires C, 32.34; H, 4.52; N, 25.14%.

후처리

  1. customThe solution was evaporated in vacuo and co-distilled with methanol and toluene
  2. customRecrystallisation of the residue with ethanol-water

출처 및 근거

ORD 기록
ord-9d454bb5525d45ecb4e7569d358a305b
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05055458

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