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Isobutylamine → 2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid isobutyl-amide

HRID 1677371
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HRID 1677371 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[N:14]=[C:15]3[C:21]([C:22]([OH:24])=O)=[CH:20][NH:19][C:16]3=[N:17][CH:18]=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].[CH2:25]([NH2:29])[CH:26]([CH3:28])[CH3:27].O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC>CN(C=O)C.C(Cl)Cl>[NH4+:14].[OH-:2].[CH2:25]([NH:29][C:22]([C:21]1[C:15]2[C:16](=[N:17][CH:18]=[C:13]([C:5]3[CH:6]=[C:7]([O:11][CH3:12])[C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=3)[N:14]=2)[NH:19][CH:20]=1)=[O:24])[CH:26]([CH3:28])[CH3:27]
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참가 물질

8

반응물 4

HCID 6558IsobutylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 595407962-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid

생성물 2

HCID 14923Ammonium Hydroxide
HCID 49764442
2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid isobutyl-amide
수율 109.3%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 6344Dichloromethane용매

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온도
70 °C

실험 절차

A mixture of 2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (70 mg, 0.2 mmol), isobutylamine (44 μL, 0.42 mmol), 1-hydroxybenzotriazole hydrate (56 mg, 0.41 mmol), and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (84 mg, 0.44 mmol) in DMF and CH2Cl2 was stirred at 70° C. overnight and partitioned between saturated NH4Cl and CH2Cl2. The aqueous layer was extracted with CH2Cl2 and the combined organic phases were washed with water, dried (Na2SO4), and concentrated. The residue was purified by preparative thin layer chromatography using 90:9.5:0.5 CH2Cl2:MeOH:concentrated aqueous NH4OH as eluant to afford 42 mg (50%) of 2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid isobutyl-amide as a pale yellow powder. M+H 403.

후처리

  1. custompartitioned between saturated NH4Cl and CH2Cl2
  2. extractionThe aqueous layer was extracted with CH2Cl2
  3. washthe combined organic phases were washed with water
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated
  6. customThe residue was purified by preparative thin layer chromatography

출처 및 근거

ORD 기록
ord-a0c9b8023de347eb8a987fab0773b396
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08008298B2

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