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Propargylamine → HCID 20165017, 화합물

HRID 255876
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HRID 255876 반응식
[CH2:1]([NH2:4])[C:2]#[CH:3].Cl.Cl[CH2:7][CH2:8][NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:19])([F:18])[F:17])[CH:11]=1>C(Cl)Cl>[CH2:1]([NH:4][CH2:7][CH2:8][NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:17])([F:18])[F:19])[CH:11]=1)[C:2]#[CH:3]
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참가 물질

4

반응물 2

HCID 239041PropargylamineHCID 20165021HCID 20165021, 화합물

생성물 1

HCID 20165017HCID 20165017, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

16.5 g of (0.3 mol) of propargylamine were dissolved in 100 ml of absolute methylene chloride, and the solution was admixed at room temperature in portions with the N-(2-chloro-ethyl)-3-(trifluoromethyl)-aniline hydrochloride obtained in step 3.1. While monitoring by chromatography, the mixture was heated until the reaction had gone to completion. After the reaction had ended, the reaction solution were extracted with the calculated quantity of sodium carbonate solution. After drying with sodium sulfate, the organic phase was evaporated under reduced pressure. The oily base thus obtained was used as such in the next step. (If this product contains significant impurities, it is advisable to recrystallize as its dihydrochloride).

후처리

  1. temperaturethe mixture was heated until the reaction
  2. extractionthe reaction solution were extracted with the calculated quantity of sodium carbonate solution
  3. dry with materialAfter drying with sodium sulfate
  4. customthe organic phase was evaporated under reduced pressure
  5. customThe oily base thus obtained
  6. customto recrystallize as its dihydrochloride)

출처 및 근거

ORD 기록
ord-fda01db0b2734bb28c5b39c924e606d5
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04699910

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