Sodium Iodide → {5-[(2-Chloro-5-nitro-phenylamino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl}-methyl-amine

HRID 1441277노트

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HRID 1441277 반응식
Cl.Cl[CH2:3][C:4]1[C:5]([NH:12][CH3:13])=[N:6][C:7]([S:10][CH3:11])=[N:8][CH:9]=1.[I-].[Na+].[Cl:16][C:17]1[CH:22]=[CH:21][C:20]([N+:23]([O-:25])=[O:24])=[CH:19][C:18]=1[NH2:26]>C(#N)C>[Cl:16][C:17]1[CH:22]=[CH:21][C:20]([N+:23]([O-:25])=[O:24])=[CH:19][C:18]=1[NH:26][CH2:3][C:4]1[C:5]([NH:12][CH3:13])=[N:6][C:7]([S:10][CH3:11])=[N:8][CH:9]=1

참가 물질

5

반응물 3

HCID 5238Sodium IodideHCID 226912-Chloro-5-nitroanilineHCID 21988143(5-Chloromethyl-2-methylsulfanyl-pyrimidin-4-yl)-methyl-amine hydrochloride

생성물 1

HCID 68700288{5-[(2-Chloro-5-nitro-phenylamino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl}-methyl-amine수율 97%

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

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온도
0 °C

실험 절차

15.85 g (5-Chloromethyl-2-methylsulfanyl-pyrimidin-4-yl)-methyl-amine hydrochloride, 1.979 g sodium iodide, and 34.49 mL N—N-diisopropylethylamine were solved in 150 ml acetonitrile and cooled to 0° C. 17.085 g 2-Chloro-5-nitrophenylamine dissolved in 150 ml acetonitrile were added slowly under stirring. The reaction mixture was stirred at room temperature for 48 hrs, then the solvent was evaporated. The residue was solved in a mixture of water/acetic acid ethyl ester (1:1), stirred and the crystalline product was sucked off and dried for 48 h under vacuum at 40° C. The two phases of the mother liquor were separated and the aqueous phase was extracted with dichloromethane. The organic phases were combined, dried over sodium sulfate, the solvent was evaporated and the residue was rubbed with diethyl ether. Both residues were combined and gave of the title product in 97% yield.

후처리

  1. additionwere added slowly
  2. stirringThe reaction mixture was stirred at room temperature for 48 hrs
  3. customthe solvent was evaporated
  4. additionThe residue was solved in a mixture of water/acetic acid ethyl ester (1:1)
  5. stirringstirred
  6. customdried for 48 h under vacuum at 40° C
  7. customThe two phases of the mother liquor were separated
  8. extractionthe aqueous phase was extracted with dichloromethane
  9. dry with materialdried over sodium sulfate
  10. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-a7ffede59ec546858625a703cfd9251e
출처 데이터셋
uspto-grants-2010_02
특허 번호
US07655651B2

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