Hydrochloric Acid → HCID 178468757, 화합물

HRID 505912

반응식

HRID 505912 반응식
[NH2:1][C:2]1[C:12]([NH2:13])=[CH:11][CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].[N:14]1([C:19]2[CH:26]=[CH:25][C:22]([CH:23]=O)=[CH:21][CH:20]=2)[CH:18]=[CH:17][N:16]=[CH:15]1.Cl.O.[S-2].[Na+].[Na+]>CO.O.C([O-])(=O)C.[Cu+2].C([O-])(=O)C.C(O)(=O)C>[N:14]1([C:19]2[CH:26]=[CH:25][C:22]([C:23]3[NH:1][C:2]4[C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])=[CH:9][CH:10]=[CH:11][C:12]=4[N:13]=3)=[CH:21][CH:20]=2)[CH:18]=[CH:17][N:16]=[CH:15]1

참가 물질

9

반응물 4

HCID 313Hydrochloric AcidHCID 7365304-(1H-imidazol-1-yl)benzaldehydeHCID 11171330Ethyl 2,3-diaminobenzoateHCID 19906495Sodium sulfide monohydrate

생성물 1

HCID 178468757HCID 178468757, 화합물

시약·촉매·용매 4

HCID 8895Cupric acetate촉매HCID 176Acetic Acid용매HCID 887Methanol용매2회HCID 962Water용매2회

반응 조건

온도
50 °C

실험 절차

1 g (5.5 mmol) of ethyl 2,3-diaminobenzoate and 0.7 ml of concentrated acetic acid were dissolved in 13 ml of methanol. 1.24 g (7.2 mmol) of 4-imidazol-1-ylbenzaldehyde, dissolved in 25 ml of methanol, were then added dropwise over a period of 30 minutes. 1.4 g (7.2 mmol) of copper(II) acetate, dissolved in 19 ml of warm water, were then rapidly added dropwise, and the entire mixture was subsequently refluxed for 20 minutes. The reaction solution was cooled to 50° C. and 2.25 ml of 32% strength hydrochloric acid were added. This was followed by careful dropwise addition of a solution of 2.13 g of sodium sulfide hydrate in 15 ml of water, and the entire mixture was stirred for another 15 minutes. The reaction solution was poured into ice-water and the resulting precipitate was filtered off with suction. The filtrate was made alkaline using aqueous sodium bicarbonate solution and extracted repeatedly with ethyl acetate. The ethyl acetate phase was separated off, dried and concentrated under reduced pressure. This gave 1.7 g of the intermediate.

후처리

  1. additionwere then added dropwise over a period of 30 minutes
  2. additionwere then rapidly added dropwise
  3. temperaturethe entire mixture was subsequently refluxed for 20 minutes
  4. filtrationthe resulting precipitate was filtered off with suction
  5. extractionextracted repeatedly with ethyl acetate
  6. customThe ethyl acetate phase was separated off
  7. customdried
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-dab53d02ab754cfbaa0a787a6ae807b6
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07781596B1

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