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Bromotrimethylsilane → 9-(4-Phosphonobutoxy)guanine

HRID 373904
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HRID 373904 반응식
C([O:3][P:4]([CH2:9][CH2:10][CH2:11][CH2:12][O:13][N:14]1[CH:22]=[N:21][C:20]2[C:19](=[O:23])[NH:18][C:17]([NH2:24])=[N:16][C:15]1=2)([O:6]CC)=[O:5])C.Br[Si](C)(C)C>CN(C)C=O>[P:4]([CH2:9][CH2:10][CH2:11][CH2:12][O:13][N:14]1[CH:22]=[N:21][C:20]2[C:19](=[O:23])[NH:18][C:17]([NH2:24])=[N:16][C:15]1=2)([OH:5])([OH:6])=[O:3]
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참가 물질

4

반응물 2

HCID 76113BromotrimethylsilaneHCID 1360386719-[4-(Diethoxyphosphoryl)butoxy]guanine

생성물 1

HCID 1354468459-(4-Phosphonobutoxy)guanine수율 65%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
23 °C

실험 절차

9-[4-(Diethoxyphosphoryl)butoxy]guanine (0.12 g, 0.33 mmol) and bromotrimethylsilane (0.43 ml, 3.3 mmol) were dissolved in dimethylformamide (5 ml) and the reaction mixture was stirred at 23° C. for 3 hr. The solvent was evaporated under vacuum and the residue dissolved in methanol:water solution (9:1). The pH of the resulting solution was adjusted to 7.0 with diluted aq. ammonia and the solvents were evaporated to dryness. The product was purified by reversed phase chromatography (eluted with water) to give the title compound (65 mg, 64%) m.p. 208° C. (water), as its ammonium salt. 1H NMR: δH ((CD3)2, SO+D2O) 1.40 (2H, m, CH2P), 1.68 (4H, br.s, CH2CH2), 4.21 (2H, m, NOCH2), 7.89 (1H, s, H-8).

후처리

  1. customThe solvent was evaporated under vacuum
  2. dissolutionthe residue dissolved in methanol
  3. customthe solvents were evaporated to dryness
  4. customThe product was purified by reversed phase chromatography (eluted with water)

출처 및 근거

ORD 기록
ord-cb72c9956e6f4377bc53dae651f93ba3
출처 데이터셋
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05166198

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