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Ammonium Chloride → ethyl 3-{[(4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}phenyl)carbonyl](methyl)amino}propanoate

HRID 2091306
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HRID 2091306 반응식
Cl[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)N(C)[C:6]([CH:12]([NH:19][C:20]1[CH:28]=[CH:27][C:23]([C:24](O)=O)=[CH:22][CH:21]=1)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[CH:5]2.[CH3:29][NH:30][CH2:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34].[OH2:38].ON1C2C=CC=C[C:43]=2N=N1.[ClH:49].C(N=C=NCCCN(C)C)C.[Cl-].[NH4+:62]>CN(C)C=O.C(N(CC)CC)C>[Cl:49][C:9]1[CH:8]=[C:4]2[C:3](=[CH:2][CH:10]=1)[N:62]([CH3:43])[C:6]([CH:12]([NH:19][C:20]1[CH:21]=[CH:22][C:23]([C:24]([N:30]([CH3:29])[CH2:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])=[O:38])=[CH:27][CH:28]=1)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[CH:5]2
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참가 물질

8

반응물 5

HCID 25517Ammonium ChlorideHCID 541480Ethyl 3-(methylamino)propanoateHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 667778124-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoic acid

생성물 1

HCID 68627241
ethyl 3-{[(4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}phenyl)carbonyl](methyl)amino}propanoate
수율 61%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 8471Triethylamine용매

실험 절차

To a mixture of 4-{[1-(5-chloro-1-methyl-1H-indol-2-yl)heptyl]amino}benzoic acid (300 mg) synthesized in Example A140(3), ethyl 3-(methylamino)propanoate (148 mg), 1-hydroxybenzotriazole monohydrate (173 mg), triethylamine (158 μL) and N,N-dimethylformamide (10 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (217 mg), and the mixture was stirred overnight at room temperature. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30-70% ethyl acetate/hexane) to give the title object compound (235 mg, 61%) as a pale-yellow oil.

후처리

  1. customto quench
  2. customthe reaction
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. washThe extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (30-70% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-db03a782759a452c80e197a5eec84184
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436043B2

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