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Sodium Bicarbonate → HCID 178422954, 화합물

HRID 1349959
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HRID 1349959 반응식
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[O:12][CH2:13][CH2:14][N:15]2[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]2)[N:3]=1.[N:21]1[C:25]2[CH:26]=[CH:27][CH:28]=[C:29]([CH:30]=O)[C:24]=2[NH:23][CH:22]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C([O-])(O)=O.[Na+]>ClCCCl>[N:21]1[C:25]2[CH:26]=[CH:27][CH:28]=[C:29]([CH2:30][N:18]3[CH2:19][CH2:20][N:15]([CH2:14][CH2:13][O:12][C:8]4[CH:7]=[CH:6][CH:5]=[C:4]5[C:9]=4[CH:10]=[CH:11][C:2]([CH3:1])=[N:3]5)[CH2:16][CH2:17]3)[C:24]=2[NH:23][CH:22]=1
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참가 물질

6

반응물 4

HCID 516892Sodium BicarbonateHCID 5049666Sodium triacetoxyborohydrideHCID 112542672-Methyl-5-(2-piperazin-1-ylethoxy)quinolineHCID 178519440HCID 178519440, 화합물

생성물 1

HCID 178422954HCID 178422954, 화합물수율 22%

시약·촉매·용매 1

HCID 11
1,2-Dichloroethane
용매

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온도
20 °C

실험 절차

A mixture of 2-methyl-5-(2-piperazin-1-ylethoxy)quinoline (0.04 g, 0.15 mmol) and 3H-benzimidazole-4-carboxaldehyde (0.024 g, 0.15 mmol) in 1,2-dichloroethane (5 mL) was treated with sodium triacetoxyborohydride (47 mg, 0.22 mmol) and stirred at 20° C. under an atmosphere of argon for 24 h. The mixture was then treated with saturated aqueous NaHCO3 (20 mL) and the organic layer separated and purified directly by chromatography on silica (ethyl acetate to 10% methanol/ethyl acetate), to afford the title compound (0.013 g, 22%) as a solid.

후처리

  1. customthe organic layer separated
  2. custompurified directly by chromatography on silica (ethyl acetate to 10% methanol/ethyl acetate)

출처 및 근거

ORD 기록
ord-a49a168b902343999f9c63cb36a62fe6
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07214674B2

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