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Dimethylformamide → HCID 86631460, 화합물

HRID 660028
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HRID 660028 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][C:6](C=O)=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[H-].[Na+].[C:14]([O:18][C:19]([N:21]1[CH2:26][CH2:25][CH:24]([CH2:27][CH2:28][CH2:29][CH2:30]OS(C)(=O)=O)[CH2:23][CH2:22]1)=[O:20])([CH3:17])([CH3:16])[CH3:15].CN([CH:39]=[O:40])C>C(Cl)(Cl)Cl>[C:14]([O:18][C:19]([N:21]1[CH2:22][CH2:23][CH:24]([CH2:27][CH2:28][CH2:29][CH2:30][N:1]2[C:9]3[C:4](=[C:5]([CH:39]=[O:40])[CH:6]=[CH:7][CH:8]=3)[CH:3]=[CH:2]2)[CH2:25][CH2:26]1)=[O:20])([CH3:15])([CH3:16])[CH3:17]
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참가 물질

6

반응물 4

HCID 6228Dimethylformamide2회HCID 24758Sodium hydrideHCID 589040Indole-5-carboxaldehydeHCID 27846694-(4-Methanesulfonyloxy-butyl)-piperidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 86631460HCID 86631460, 화합물

시약·촉매·용매 1

HCID 6212
Chloroform
용매

실험 절차

To a 0° C. solution of 1H-indole-5-carbaldehyde (0.43 g, 2.96 mmol) in DMF (10 mL) was added NaH (60% in mineral oil; 0.14 mg, 3.55 mmol). After 45 min at 0° C., a solution of 4-(4-methanesulfonyloxy-butyl)-piperidine-1-carboxylic acid tert-butyl ester (1.00 g, 3.15 mmol) in DMF (5 mL) was added dropwise. The mixture was warmed to rt and stirred for 18 h. The mixture was diluted with CHCl3 (20 mL) and washed with water (15 mL). The organic layer was dried and concentrated to obtain the crude residue, which was used purified by FCC to give 0.96 g (88%). MS: mass calcd. for C22H30N2O3, 370.23; m/z found, 371.4 [M+H]+.

후처리

  1. washwashed with water (15 mL)
  2. customThe organic layer was dried
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-955e79c016a3447fb3e350f9e5302160
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084466B2

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