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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 15580707, 화합물 → HCID 15580720, 화합물

HRID 543804
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HRID 543804 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[CH2:13][CH2:12][C:11]([NH:14][C:15](=[O:20])C(F)(F)F)=[N:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8].ClC1C=C(N2CC(C)C(NC=O)=N2)C=CC=1Cl>C(O)=O>[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[CH2:13][CH2:12][C:11]([NH:14][CH:15]=[O:20])=[N:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 15580707HCID 15580707, 화합물HCID 15580721HCID 15580721, 화합물

생성물 1

HCID 15580720HCID 15580720, 화합물

시약·촉매·용매 1

HCID 284Formic Acid용매

실험 절차

A mixture of 5.0 g. of 3-amino-1-(3,4-dichlorophenyl)-2-pyrazoline (prepared in Example 1) and 25 ml. of a mixture of formic acid and acetic anhydride (Example 15) is allowed to stand at room temperature for one hour. The resulting solid is collected by filtration and washed with hexane. The solid is dissolved in dichloromethane and is columnized and recrystallized as described in Example 5 to give 3.85 g. of the desired product as yellow prisms, m.p. 151°-153° C.

후처리

  1. additionA mixture of 5.0 g
  2. filtrationThe resulting solid is collected by filtration
  3. washwashed with hexane
  4. dissolutionThe solid is dissolved in dichloromethane
  5. customrecrystallized
  6. customto give 3.85 g

출처 및 근거

ORD 기록
ord-a3936648f46947568829f3767ab788d1
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04447442

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