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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Malonic Acid → HCID 68714384, 화합물

HRID 1873762
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HRID 1873762 반응식
[CH3:1][C:2]1[N:3]=[C:4]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[S:5][C:6]=1[CH:7]=O.C(O)(=O)[CH2:16][C:17]([OH:19])=[O:18].N1CCCCC1>N1C=CC=CC=1>[CH3:1][C:2]1[N:3]=[C:4]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[S:5][C:6]=1[CH:7]=[CH:16][C:17]([OH:19])=[O:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 867Malonic AcidHCID 8082PiperidineHCID 27954914-methyl-2-phenyl-1,3-thiazole-5-carbaldehyde

생성물 1

HCID 68714384HCID 68714384, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

반응 조건

온도
100 °C

실험 절차

A mixture of 300 mg (1.47 mmol) of 4-methyl-2-phenyl-thiazole-5-carbaldehyde, 169 mg (1.62 mmol) of malonic acid and 880 mg (10.33 mmol) of piperidine in 10 ml of pyridine was stirred at 90° C. for 5 h and at 100° C. for 6 h. After concentration, the residue was treated with a sodium hydrogencarbonate solution and ethyl acetate. The aqueous phase was separated and acidified. The precipitated product was filtered off with suction and dried. Yield: 260 mg.

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후처리

  1. concentrationAfter concentration
  2. additionthe residue was treated with a sodium hydrogencarbonate solution and ethyl acetate
  3. customThe aqueous phase was separated
  4. filtrationThe precipitated product was filtered off with suction
  5. customdried

출처 및 근거

ORD 기록
ord-e2683a4197b543759148cb397b8fe8ea
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08304438B2

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