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Water → 1-[2-(Trifluoromethyl)pyrimidin-5-yl]methanamine

HRID 1181438
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HRID 1181438 반응식
[N:1]([CH2:4][C:5]1[CH:6]=[N:7][C:8]([C:11]([F:14])([F:13])[F:12])=[N:9][CH:10]=1)=[N+]=[N-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>C1COCC1>[NH2:1][CH2:4][C:5]1[CH:6]=[N:7][C:8]([C:11]([F:14])([F:13])[F:12])=[N:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 11776TriphenylphosphineHCID 858698555-Azidomethyl-2-(trifluoromethyl)pyrimidine

생성물 1

HCID 450733911-[2-(Trifluoromethyl)pyrimidin-5-yl]methanamine수율 55.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 5-(azidomethyl)-2-(trifluoromethyl)pyrimidine (Description 120; 660 mg, 3.26 mmol) in anhydrous THF (10 ml) was added triphenylphosphine (1.71 g, 6.52 mmol) and water (0.059 ml, 3.26 mmol) and the resulting mixture stirred at room temperature overnight. The mixture was evaporated and the residue purified by column chromatography on silica elution with 5% MeOH in DCM+0.5% NH4OH to give the title compound (320 mg, 55%) as a pale yellow solid.

후처리

  1. customThe mixture was evaporated
  2. customthe residue purified by column chromatography on silica elution with 5% MeOH in DCM+0.5% NH4OH

출처 및 근거

ORD 기록
ord-64469a26665d4d448894d148df3eac04
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07285563B2

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