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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 21114633, 화합물

HRID 1767708
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HRID 1767708 반응식
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([F:9])=[CH:4][N:3]=1.C(N(CC)CC)C.[C:17]([NH2:20])#[C:18][CH3:19].O>C(#N)C>[Cl:1][C:2]1[N:7]=[C:6]([NH:20][CH2:17][C:18]#[CH:19])[C:5]([F:9])=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8471TriethylamineHCID 17140Prop-1-yn-1-amineHCID 2507052,4-Dichloro-5-fluoropyrimidine

생성물 1

HCID 21114633HCID 21114633, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

11.1 g (66 mmol) of 2,4-dichloro-5-fluoropyrimidine is dissolved in 60 ml of acetonitrile, and 10.2 ml (73 mmol) of triethylamine and 6.0 ml (86 mmol) of propynylamine are added. The reaction mixture is stirred overnight at room temperature and then poured into water. The mixture is extracted by means of ethyl acetate, the combined organic phases are dried on MgSO2, and the solvent is evaporated by means of underpressure. After the remaining material is recrystallized with diisopropyl ether/hexane, the yield is 10.6 g (87% of theory) of the product.

후처리

  1. extractionThe mixture is extracted by means of ethyl acetate
  2. customthe combined organic phases are dried on MgSO2
  3. customthe solvent is evaporated by means of underpressure
  4. customAfter the remaining material is recrystallized with diisopropyl ether/hexane

출처 및 근거

ORD 기록
ord-5e9f1a40f8fc4bfb81006ccb6c3f0c68
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07235561B2

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