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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,1'-Carbonyldiimidazole → 2H-Benzimidazol-2-one, 1,3-dihydro-1-(2-methoxyethyl)-

HRID 1096656
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HRID 1096656 반응식
[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[C:7]([NH2:12])=[CH:8][CH:9]=[CH:10][CH:11]=1.C1N=CN([C:18](N2C=NC=C2)=[O:19])C=1>C1COCC1>[CH3:1][O:2][CH2:3][CH2:4][N:5]1[C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[NH:12][C:18]1=[O:19]
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참가 물질

4

반응물 2

HCID 682631,1'-CarbonyldiimidazoleHCID 102614521-N-(2-methoxyethyl)benzene-1,2-diamine

생성물 1

HCID 99901412H-Benzimidazol-2-one, 1,3-dihydro-1-(2-methoxyethyl)-수율 92%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

The residue 109B (422 mg, 2.54 mmol) was dissolved in THF (7.5 mL). CDI (494 mg, 3.05 mmol) in THF (7.6 mL) was added slowly via addition funnel. After addition the mixture was stirred overnight at room temperature, solvent was removed under vacuum. The residue was purified by column chromatography (5% MeOH/DCM) to give the product 1-(2-methoxyethyl)-1H-benzo[d]imidazol-2(3H)-one (109C) as an orange solid (449 mg, 92%). ESI-MS:m/z 193.3 (M+H)+.

후처리

  1. additionAfter addition the mixture
  2. customsolvent was removed under vacuum
  3. customThe residue was purified by column chromatography (5% MeOH/DCM)

출처 및 근거

ORD 기록
ord-4ede0777ad9f4c1ba9201627499b8712
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08138168B1

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