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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 178511051, 화합물

HRID 1417321
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인쇄 미리보기

반응식

HRID 1417321 반응식
C[N:2](C)/[CH:3]=[CH:4]/[C:5]([C:7]1[CH:28]=[CH:27][C:10]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][N:16]2C(=O)C3C(=CC=CC=3)C2=O)=[CH:9][CH:8]=1)=O.[NH2:30]N.Cl>C(O)C>[NH:2]1[CH:3]=[CH:4][C:5]([C:7]2[CH:28]=[CH:27][C:10]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][NH2:16])=[CH:9][CH:8]=2)=[N:30]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 9321HydrazineHCID 67693872(E)-2-[4-[4-[3-(dimethylamino)-1-oxo-2-propenyl]phenoxy]butyl]-1H-isoindole-1,3(2H)-dione

생성물 1

HCID 178511051HCID 178511051, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

A suspension of 21.2 g of (E)-2-[4-[4-[3-(dimethylamino)-1-oxo-2-propenyl]phenoxy]butyl]-1H-isoindole-1,3(2H)-dione (Example 48) in 300 ml of boiling ethanol is treated with 6 ml of anhydrous hydrazine. A suspension quickly develops, necessitating addition of 200 ml more ethanol to permit stirring. While stirring 35 ml of concentrated HCl is then added, the mixture refluxed a further hour, and filtered hot. The insolubles are washed with 200 ml of boiling water. The combined filtrates are taken to dryness in vacuo, leaving the hydrochloride salt of the title compound as shown by mass spectrometry. The product is utilized for synthesis without further purification.

후처리

  1. additionis then added
  2. temperaturethe mixture refluxed a further hour
  3. filtrationfiltered hot
  4. washThe insolubles are washed with 200 ml of boiling water

출처 및 근거

ORD 기록
ord-08b8c687defc4f8992f3b72deabcfd69
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05877196

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