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Methyl iodide → HCID 178503548, 화합물

HRID 733183
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반응식

HRID 733183 반응식
[CH2:1]([O:8][CH2:9][CH2:10][CH2:11][C:12]1[N:17]=[C:16]([SH:18])[N:15]=[C:14]([OH:19])[CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+].[CH3:22]I>>[CH2:1]([O:8][CH2:9][CH2:10][CH2:11][C:12]1[N:17]=[C:16]([S:18][CH3:22])[N:15]=[C:14]([OH:19])[CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6328Methyl iodideHCID 14797Potassium HydroxideHCID 178516034HCID 178516034, 화합물

생성물 1

HCID 178503548HCID 178503548, 화합물

실험 절차

A mixture of 6-(3-benzyloxy-propyl)-2-mercapto-pyrimidin-4-ol (7.94 g), potassium hydroxide (32 mL of 1N solution in methanol) and methyl iodide (1.97 mL) was stirred at room temperature overnight. The precipitate was filtered, washed successively with methanol (2×20 mL), isopropanol (2×20 mL) and water (2×20 mL), then dried to afford 6-(3-benzyloxy-propyl)-2-methylsulfanyl-pyrimidin-4-ol as a white powder (7.0 g). MS m/z 291.0 (M+1), 100%.

후처리

  1. filtrationThe precipitate was filtered
  2. washwashed successively with methanol (2×20 mL), isopropanol (2×20 mL) and water (2×20 mL)
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
custom
dried

출처 및 근거

ORD 기록
ord-3bea2f0adca94fc8b613d0da6aa42aa7
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589095B2

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