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HCID 3010392, 화합물 → 4-Amino-5-bromo-7-(2-hydroxyethoxymethyl)pyrrolo(2,3-d)pyrimidine

HRID 1651083
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인쇄 미리보기

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HRID 1651083 반응식
Cl[C:2]1[C:3]2[C:10]([Br:11])=[CH:9][N:8]([CH2:12][O:13][CH2:14][CH2:15][OH:16])[C:4]=2[N:5]=[CH:6][N:7]=1.[NH3:17].N>CO>[NH2:17][C:2]1[C:3]2[C:10]([Br:11])=[CH:9][N:8]([CH2:12][O:13][CH2:14][CH2:15][OH:16])[C:4]=2[N:5]=[CH:6][N:7]=1
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참가 물질

4

반응물 2

HCID 3010392HCID 3010392, 화합물HCID 6857397HCID 6857397, 화합물

생성물 1

HCID 1226824-Amino-5-bromo-7-(2-hydroxyethoxymethyl)pyrrolo(2,3-d)pyrimidine

시약·촉매·용매 1

HCID 887Methanol용매2회

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온도
125 °C

실험 절차

5-Bromo-4-chloro-7-(2-hydroxyethoxymethyl)pyrrolo [2,3-d]pyrimidine (8b, 0.7 g) was dissolved in dry methanol (10 mL) and methanol saturated with NH3 ammonia (40 mL) was then added to this solution. The reaction mixture was heated at 125 degrees C. in a sealed reaction vessel for 10 hours. The solvent was removed at 40 degrees under reduced pressure and the resulting solid was then subjected to column chromatography. Elution of the silica gel column (20×3 cm) with 5% MeOH in CHCl3 yielded a solid after evaporation of the appropriate UV absorbing fractions. This solid was recrystallized from CHCl3 to afford 11, 0.18 g (31.25%), mp 163-164 degrees C. 1H-NMR (DMSO-d6): δ 8.13 (s, 1, C2-H), 7.55 (s, 1, C6-H), 6.81 (bs, 2, exchangeable with D2O, NH2), 5.5 (s, 2, N7-CH2), 4.62 (m, 1, exchangeable with D2O, OH), 3.42 (m, 4, CH2): UVλmax nm (ε×104) (pH 7) 211 (1.9), 278 (0.9); (pH 1) 233 (2.0), 280 (0.94); (pH 11) 227 (0.9), 278 (0.95).

후처리

  1. customin a sealed reaction vessel for 10 hours
  2. customThe solvent was removed at 40 degrees under reduced pressure
  3. washElution of the silica gel column (20×3 cm) with 5% MeOH in CHCl3
  4. customyielded a solid
  5. customafter evaporation of the appropriate UV
  6. customabsorbing fractions
  7. customThis solid was recrystallized from CHCl3

출처 및 근거

ORD 기록
ord-08db7aaafa484f8cbc1374f3b6e95d24
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04927830

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