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Diisopropylethylamine → HCID 21034893, 화합물

HRID 1833246
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HRID 1833246 반응식
Cl.[CH2:2]([O:4][C:5](=[O:19])[CH:6]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([O:17][CH3:18])[CH:10]=1)[CH2:7][NH2:8])[CH3:3].[CH:20]([O:24][C:25]1[CH:26]=[C:27]([CH2:31][C:32](O)=[O:33])[CH:28]=[CH:29][CH:30]=1)([CH2:22][CH3:23])[CH3:21].CN(C(ON1N=NC2C1=CC=CC=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C>CN(C)C=O.C(OCC)(=O)C.C(OCC)(=O)C.CCCCCC>[CH2:2]([O:4][C:5](=[O:19])[CH:6]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([O:17][CH3:18])[CH:10]=1)[CH2:7][NH:8][C:32](=[O:33])[CH2:31][C:27]1[CH:28]=[CH:29][CH:30]=[C:25]([O:24][CH:20]([CH2:22][CH3:23])[CH3:21])[CH:26]=1)[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 81531DiisopropylethylamineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 22048444HCID 22048444, 화합물HCID 69551005Ethyl 3-amino-2-(3,4-dimethoxyphenyl)propanoate hydrochloride

생성물 1

HCID 21034893HCID 21034893, 화합물수율 98%

시약·촉매·용매

3
HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매HCID 21226206Ethyl acetate hexane용매

실험 절차

To a stirred solution 3-amino-2-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester hydrochloride (6.5 g, 25.8 mmol) and (3-sec-butoxy-phenyl)-acetic acid (5.9 g, 28.4 mmol) in N,N-dimethylformamide (130 mL) was added O-benzotriazole-N,N,N′,N′-tetramethyl-uronium hexaflurophosphate (HBTU) (11.8 g, 31.1 mmol) and diisopropylethylamine (14.8 mL, 85.0 mmol). The reaction mixture was stirred at room temperature for 15 hrs. The solvent was evaporated and the residue was diluted with ethyl acetate and saturated sodium bicarbonate solution. The aqueous phase was extracted with ethyl acetate (3×100 mL). The combined extracts were washed with 1N hydrogen chloride solution (50 mL), water (50 mL), saturated aqueous sodium chloride solution (50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70–230 mesh, 40% ethyl acetate/hexane, 100% ethyl acetate) afforded 3-[2-(3-sec-butoxy-phenyl)-acetylamino]-2-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester (11.2 g, 98% yield) as a red oil.

후처리

  1. customThe solvent was evaporated
  2. additionthe residue was diluted with ethyl acetate and saturated sodium bicarbonate solution
  3. extractionThe aqueous phase was extracted with ethyl acetate (3×100 mL)
  4. washThe combined extracts were washed with 1N hydrogen chloride solution (50 mL), water (50 mL), saturated aqueous sodium chloride solution (50 mL)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-5c0ab5006974446ea9574d1fb2aa6926
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067529B2

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