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4-Chlorobenzylamine → HCID 178522935, 화합물

HRID 1978923
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인쇄 미리보기

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HRID 1978923 반응식
[OH:1][C:2]1[C:7]([C:8]([O:10]CC)=O)=[CH:6][N:5]=[C:4]2[S:13][CH:14]=[CH:15][C:3]=12.[Cl:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21][NH2:22])=[CH:19][CH:18]=1>C1(C)C=CC=CC=1>[Cl:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21][NH:22][C:8]([C:7]2[C:2]([OH:1])=[C:3]3[CH:15]=[CH:14][S:13][C:4]3=[N:5][CH:6]=2)=[O:10])=[CH:19][CH:18]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 660364-ChlorobenzylamineHCID 178469713HCID 178469713, 화합물

생성물 1

HCID 178522935HCID 178522935, 화합물수율 45%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
190 °C

실험 절차

A mixture of ethyl 4-hydroxythieno[2,3-b]pyridine-5-carboxylate (J. Heterocyclic Chem. 1977, 14, 807) (0.447 g) and 4-chlorobenzylamine (2.43 mL) is stirred at 190° C. for 1 h. The reaction is then allowed to cool to rt and is diluted with toluene (5 mL). The resulting precipitate is filtered off and washed with toluene followed by hexanes to yield an off-white solid. This material is recrystallized from acetic acid/water then ethanol to yield 0.285 g (45%) of the title compound as a white solid.

후처리

  1. temperatureto cool to rt
  2. filtrationThe resulting precipitate is filtered off
  3. washwashed with toluene
  4. customto yield an off-white solid
  5. customThis material is recrystallized from acetic acid/water

출처 및 근거

ORD 기록
ord-5e4fe1b6bb45439e902dc0c40e4e6197
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06239142B1

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