Diethyl Ether → 2-[(1-Methoxymethoxy-5,6,7,8-tetrahydro-naphthalene-2-carbonyl)-amino]-2-methyl-propionic acid methyl ester

HRID 874750노트

반응식

HRID 874750 반응식
[CH3:1][O:2][CH2:3][O:4][C:5]1[C:14]2[CH2:13][CH2:12][CH2:11][CH2:10][C:9]=2[CH:8]=[CH:7][C:6]=1[C:15]([OH:17])=O.Cl.[CH3:19][O:20][C:21](=[O:26])[C:22]([NH2:25])([CH3:24])[CH3:23].C(N(CC)C(C)C)(C)C.C(OCC)C>CN(C)C=O.O>[CH3:19][O:20][C:21](=[O:26])[C:22]([NH:25][C:15]([C:6]1[CH:7]=[CH:8][C:9]2[CH2:10][CH2:11][CH2:12][CH2:13][C:14]=2[C:5]=1[O:4][CH2:3][O:2][CH3:1])=[O:17])([CH3:24])[CH3:23]

참가 물질

7

실험 절차

In a round bottom flask was placed 0.96 g 1-methoxymethoxy-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid, 1.25 g 2-amino-2-methyl-propionic acid methyl ester hydrochloride, 3.09 g of O-(7-azabenzotriazole-1-yl)-N,N,N,N-tetramethyluronium hexafluoro phosphate and 2.83 ml of N,N-diisopropylethylamine in 60 ml of N,N-di-methylformamide. It was left stirring at room temperature overnight. 60 ml of diethylether and 60 ml of water were added to the reaction. The organic layer was separated and washed again with 50 ml of water. It was dried over magnesium sulphate, filtered and concentrated in vacuo to afford a crude yellow oil. Purification was performed by flash chromatography (silica, heptanes/ethyl acetate) to give 1.04 g 2-[(1-methoxymethoxy-5,6,7,8-tetrahydro-naphthalene-2-carbonyl)-amino]-2-methyl-propionic acid methyl ester.

후처리

  1. customIn a round bottom flask was placed
  2. waitIt was left
  3. customThe organic layer was separated
  4. washwashed again with 50 ml of water
  5. dry with materialIt was dried over magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customto afford a crude yellow oil
  9. customPurification

출처 및 근거

ORD 기록
ord-d74647428f34456e84d44696a4fdb1be
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08980938B2

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