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1-Methyl-2-(2-nitrophenyl)-benzimidazole-4-carboxaldehyde ethylene acetal → Benzenamine, 2-[4-(1,3-dioxolan-2-yl)-1-methyl-1H-benzimidazol-2-yl]-

HRID 843234
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HRID 843234 반응식
[CH2:1]1[O:24][CH:4]([C:5]2[C:13]3[N:12]=[C:11]([C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=4[N+:20]([O-])=O)[N:10]([CH3:23])[C:9]=3[CH:8]=[CH:7][CH:6]=2)[O:3][CH2:2]1>CO.[Pd]>[CH2:1]1[O:24][CH:4]([C:5]2[C:13]3[N:12]=[C:11]([C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=4[NH2:20])[N:10]([CH3:23])[C:9]=3[CH:8]=[CH:7][CH:6]=2)[O:3][CH2:2]1
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참가 물질

4

반응물 1

HCID 154902661-Methyl-2-(2-nitrophenyl)-benzimidazole-4-carboxaldehyde ethylene acetal

생성물 1

HCID 11346961Benzenamine, 2-[4-(1,3-dioxolan-2-yl)-1-methyl-1H-benzimidazol-2-yl]-수율 99%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A solution of 6 (0.85 g, 2.6 mmol) in 50 mL MeOH was mixed with 85 mg of Pd/C and hydrogenated with H2 at a pressure of 10 psi for 3 hours. The mixture was then filtered, and the solvent was removed to give 0.76 g (98%) of the title compound as a white solid. 1H NMR (CDCl3): δ 4.44 (s, 3H), 4.69-4.90 (m, 4H), 5.69 (broad s, 2H), 7.44 (d, J=7.8 Hz, 2H), 7.81-8.05 (m, 4H), 8.14 (d, J=1.6, 6.9 Hz, 1H); HRMS: Calcd. for C17H17N3O2 295.1321, found 295.1325.

후처리

  1. filtrationThe mixture was then filtered
  2. customthe solvent was removed

출처 및 근거

ORD 기록
ord-0324657e1c18428c935804c2c4abdf3e
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06376664B1

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