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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydroxyamine hydrochloride → 3,7-Dichloroquinoline-8-carbonitrile

HRID 615073
노트
인쇄 미리보기

반응식

HRID 615073 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:12])[C:6]=2[CH2:13]Cl.Cl.[NH2:16]O.C([O-])=O.[Na+]>C(O)=O.O>[Cl:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([Cl:12])[C:6]=2[C:13]#[N:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 2723810Sodium FormateHCID 13090784HCID 13090784, 화합물

생성물 1

HCID 130907923,7-Dichloroquinoline-8-carbonitrile

시약·촉매·용매 2

HCID 284Formic Acid용매HCID 962Water용매

실험 절차

28.1 parts of 3,7-dichloro-8-chloromethylquinoline (Example 1), 6.95 parts of hydroxylamine hydrochloride and 13.6 parts of sodium formate in 200 ml of formic acid and 60 ml of water were stirred at 100° C. for 12 hours. The reaction solution was poured onto ice and the precipitated solid was filtered off with suction, washed neutral with water and dried. 19 parts of 3,7-dichloro-8-cyanoquinoline of melting point 222° C. were obtained. The yield corresponds to 78.5% of theory.

후처리

  1. additionThe reaction solution was poured onto ice
  2. filtrationthe precipitated solid was filtered off with suction
  3. washwashed neutral with water
  4. customdried

출처 및 근거

ORD 기록
ord-e484d41706ac45d68675df1294a7149d
출처 데이터셋
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04497651

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