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HCID 11616834, 화합물 → HCID 11602341, 화합물

HRID 746620
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HRID 746620 반응식
[F:1][C:2]1[C:3]([C:8]([C:10]2[C:11]3[CH:23]=[CH:22][CH:21]=[CH:20][C:12]=3[S:13][C:14]=2[CH2:15][CH2:16][N:17]([CH3:19])[CH3:18])=[CH2:9])=[N:4][CH:5]=[CH:6][CH:7]=1>C(O)C.[Pt](=O)=O>[F:1][C:2]1[C:3]([CH:8]([C:10]2[C:11]3[CH:23]=[CH:22][CH:21]=[CH:20][C:12]=3[S:13][C:14]=2[CH2:15][CH2:16][N:17]([CH3:18])[CH3:19])[CH3:9])=[N:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 11616834HCID 11616834, 화합물2회

생성물 1

HCID 11602341HCID 11602341, 화합물

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

To a solution of (2-{3-[1-(3-fluoro-pyridin-2-yl)-vinyl]-benzo[b]thiophen-2-yl}-ethyl)-dimethyl-amine (Compound 18-2) (26 mg, 0.080 mmol) in ethanol (1 mL), platinum dioxide (9 mg, 0.04 mol) was added. The reaction was shaken at 30 psi for 4 hours under H2 atmosphere and monitored by LC/MS. The reaction was filtered and washed with EtOH and subsequently purified by mass triggered preparative HPLC to afford (2-{3-[1-(3-fluoro-pyridin-2-yl)-ethyl]-benzo[b]thiophen-2-yl}-ethyl)-dimethyl-amine (Compound 18-3). MH+=329. tR=4.7 min (Method 2).

후처리

  1. filtrationThe reaction was filtered
  2. washwashed with EtOH
  3. customsubsequently purified by mass

출처 및 근거

ORD 기록
ord-0747cf039b534587b697f4a31a708cc2
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07393865B2

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