1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → 2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl (RS)-2-(2-methylpyrimidin-5-yl)-3,3-dimethylbutanoate

HRID 1088311노트

반응식

HRID 1088311 반응식
Cl.C(N=C=NCCCN(C)C)C.[CH3:13][C:14]1[N:19]=[CH:18][C:17]([CH:20]([C:24]([CH3:27])([CH3:26])[CH3:25])[C:21]([OH:23])=[O:22])=[CH:16][N:15]=1.[CH3:28][O:29][CH2:30][C:31]1[C:38]([F:39])=[C:37]([F:40])[C:34]([CH2:35]O)=[C:33]([F:41])[C:32]=1[F:42]>ClCCl.CN(C1C=CN=CC=1)C>[CH3:13][C:14]1[N:19]=[CH:18][C:17]([CH:20]([C:24]([CH3:27])([CH3:26])[CH3:25])[C:21]([O:23][CH2:35][C:34]2[C:33]([F:41])=[C:32]([F:42])[C:31]([CH2:30][O:29][CH3:28])=[C:38]([F:39])[C:37]=2[F:40])=[O:22])=[CH:16][N:15]=1

참가 물질

6

실험 절차

A solution of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.276 g) in dry dichloromethane (6 cm3) was added to a stirred solution of (RS)-2-(2-methylpyrimidin-5-yl)-3,3-dimethylbutanoic acid (0.3 g) and 4-(methoxymethyl)-2,3,5,6-tetrafluorobenzylalcohol (0.33 g) containing a catalytic amount of 4-(N,N'-dimethylamino) pyridine. The stirred mixture was maintained at the ambient temperature for 2 hours, and left to stand overnight. The reaction solution was washed with water, dried over anhydrous magnesium sulphate and concentrated by evaporation of the solvent under reduced pressure. The residue was subjected to column chromatography on silica gel using a 1:1 (by volume) mixture of ethyl acetate and dichloromethane as eluent to give 2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl (RS)-2-(2-methylpyrimidin-5-yl)-3,3-dimethylbutanoate (0.228 g) as a yellow oil.

후처리

  1. waitleft
  2. washThe reaction solution was washed with water
  3. dry with materialdried over anhydrous magnesium sulphate
  4. concentrationconcentrated by evaporation of the solvent under reduced pressure
  5. additiona 1:1 (by volume) mixture of ethyl acetate and dichloromethane as eluent

출처 및 근거

ORD 기록
ord-c93e0e5ee1ba418abb43daff82a7a610
출처 데이터셋
uspto-grants-1990_10
특허 번호
US04962109

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