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4,4-Diethoxybutylamine → HCID 57950350, 화합물

HRID 1020702
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HRID 1020702 반응식
C(O[CH:4](OCC)[CH2:5][CH2:6][CH2:7][NH2:8])C.Cl.[Br:13][C:14]1[CH:15]=[C:16]([NH:21]N)[CH:17]=[CH:18][C:19]=1[F:20]>CO>[Br:13][C:14]1[CH:15]=[C:16]2[C:17]([C:5]([CH2:6][CH2:7][NH2:8])=[CH:4][NH:21]2)=[CH:18][C:19]=1[F:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 806724,4-DiethoxybutylamineHCID 67250486(3-Bromo-4-fluorophenyl)hydrazine hydrochloride

생성물 1

HCID 57950350HCID 57950350, 화합물수율 116.7%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
180 °C

실험 절차

4,4-Diethoxybutan-1-amine (4.72 g, 29.3 mmol) was added to (3-bromo-4-fluorophenyl)hydrazine hydrochloride (6.4 g, 27 mmol). The resulting mixture in an open round bottom flask was placed into a preheated oil bath at 180° C. The mixture was stirred at 180° C. for 2.5 h and then cooled to 120° C. Methanol (300 mL) was added, and the mixture was stirred at ambient temperature for 18 h. The resulting suspension was filtered through a silica gel plug, and the silica gel was then washed with methanol (5×300 mL). The combined methanol fractions were concentrated under vacuum to provide the crude title compound (8.1 g) as a yellow solid, which was used in the next step without further purification: ESI MS m/z 257 [M+H]+.

후처리

  1. customThe resulting mixture in an open round bottom flask was placed into a preheated oil bath at 180° C
  2. temperaturecooled to 120° C
  3. stirringthe mixture was stirred at ambient temperature for 18 h
  4. filtrationThe resulting suspension was filtered through a silica gel plug
  5. washthe silica gel was then washed with methanol (5×300 mL)
  6. concentrationThe combined methanol fractions were concentrated under vacuum

출처 및 근거

ORD 기록
ord-43f1710483614ea08ece6c672493485f
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08716308B2

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