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2-Methoxyethylamine → 2-Butoxy-8-methoxy-9-{4-[(2-methoxyethyl)amino]butyl}-9H-purine-6-amine

HRID 869344
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HRID 869344 반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][N:6]1[C:14]([O:15][CH3:16])=[N:13][C:12]2[C:7]1=[N:8][C:9]([O:18][CH2:19][CH2:20][CH2:21][CH3:22])=[N:10][C:11]=2[NH2:17].[CH3:23][O:24][CH2:25][CH2:26][NH2:27]>C(#N)C>[CH2:19]([O:18][C:9]1[N:8]=[C:7]2[C:12]([N:13]=[C:14]([O:15][CH3:16])[N:6]2[CH2:5][CH2:4][CH2:3][CH2:2][NH:27][CH2:26][CH2:25][O:24][CH3:23])=[C:11]([NH2:17])[N:10]=1)[CH2:20][CH2:21][CH3:22]
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참가 물질

4

반응물 2

HCID 80182-MethoxyethylamineHCID 231585119-(4-Bromobutyl)-2-butoxy-8-methoxyadenine

생성물 1

HCID 231585492-Butoxy-8-methoxy-9-{4-[(2-methoxyethyl)amino]butyl}-9H-purine-6-amine

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
80 °C

실험 절차

The compound obtained in Example 2-13 step (i) (500 mg) and (2-methoxyethyl)amine (303 mg) were dissolved in acetonitrile (5 ml) and stirred at 80° C. for 1 hour. The reaction mixture was cooled, filtered and purified by RPHPLC to give the titled compound as a white solid. Yield: 270 mg (55%); mp 99-100° C., MS APCI+ve 367 (M+H).

후처리

  1. temperatureThe reaction mixture was cooled
  2. filtrationfiltered
  3. custompurified by RPHPLC

출처 및 근거

ORD 기록
ord-2b29ead20b6442d8a3a35723228f41c3
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969362B2

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