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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3,7-Dichloroquinoline-8-carbonitrile → 7-(Butylamino)-3-chloroquinoline-8-carbonitrile

HRID 1980751
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HRID 1980751 반응식
[Cl:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7](Cl)[C:6]=2[C:13]#[N:14]>C(N)CCC>[CH2:3]([NH:4][C:7]1[C:6]([C:13]#[N:14])=[C:5]2[C:10]([CH:11]=[C:2]([Cl:1])[CH:3]=[N:4]2)=[CH:9][CH:8]=1)[CH2:2][CH2:11][CH3:10]
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참가 물질

3

반응물 1

HCID 130907923,7-Dichloroquinoline-8-carbonitrile

생성물 1

HCID 132065267-(Butylamino)-3-chloroquinoline-8-carbonitrile수율 150.5%

시약·촉매·용매 1

HCID 8007Butylamine용매

실험 절차

44.5 g of 3,7-dichloro-8-cyanoquinoline in 200 g of n-butylamine were heated at 80° C. for 14 hours, the solution was poured onto ice water and extracted with twice 100 ml of methylene chloride, the combined extracts were dried with Na2SO4 and evaporated down, the oily residue was treated with ether, and the precipitated solid was filtered off under suction. 39 g of 7-n-butylamino-3-chloro-8-cyanoquinoline of melting point 89° C. were obtained. Yield: 75% of theory.

후처리

  1. additionthe solution was poured onto ice water
  2. extractionextracted with twice 100 ml of methylene chloride
  3. dry with materialthe combined extracts were dried with Na2SO4
  4. customevaporated down
  5. additionthe oily residue was treated with ether
  6. filtrationthe precipitated solid was filtered off under suction

출처 및 근거

ORD 기록
ord-dc737421c13d49a0b0b64fab089ffe41
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04511393

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