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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formic Acid → HCID 15580708, 화합물

HRID 543808
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HRID 543808 반응식
FC(F)(F)[C:3]([NH:5][C:6]1[CH2:10][CH2:9][N:8]([C:11]2[CH:16]=[CH:15][C:14](C(=O)C(F)(F)F)=[CH:13][CH:12]=2)[N:7]=1)=[O:4].C(O)=O.ClC1C=C(N2CC(C)C(NC=O)=N2)C=CC=1Cl>O>[C:11]1([N:8]2[CH2:9][CH2:10][C:6]([NH:5][CH:3]=[O:4])=[N:7]2)[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 284Formic AcidHCID 15580703HCID 15580703, 화합물HCID 15580721HCID 15580721, 화합물

생성물 1

HCID 15580708HCID 15580708, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 10.0 g. of 3-amino-1-phenyl-2-pyrozoline (prepared in Example 8) and 50.0 ml. of a mixture of formic acid and acetic anhydride (Example 15) is allowed to stand at room temperature for 3 hours. Water is added and the white crystals are collected by filtration. The solid is dissolved in dichloromethane. The solution is dried over magnesium sulfate and filtered through a hydrous magnesium silicate. The filtrate is evaporated in vacuo to give pink crystals. A 500 mg. portion of crude product is recrystallized from dichloromethane-hexane to give 403 mg. of the desired product as a white solid, m.p. 140°-141° C.

후처리

  1. additionA mixture of 10.0 g
  2. filtrationthe white crystals are collected by filtration
  3. dissolutionThe solid is dissolved in dichloromethane
  4. dry with materialThe solution is dried over magnesium sulfate
  5. filtrationfiltered through a hydrous magnesium silicate
  6. customThe filtrate is evaporated in vacuo
  7. customto give pink crystals
  8. customportion of crude product is recrystallized from dichloromethane-hexane
  9. customto give 403 mg

출처 및 근거

ORD 기록
ord-03c554fcc0d24db9ac2b3c70468e5725
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04447442

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