Diisopropylethylamine → 1-{[5-Bromo-4-(3-chlorophenyl)furan-2-yl]carbonyl}imidazolidin-4-one

HRID 2190131노트

반응식

HRID 2190131 반응식
BrC1C=C(C([N:16]2C[CH2:20][NH:19][C:18](=[O:22])[CH2:17]2)=O)OC=1C1C=CC=C(Cl)C=1.[Br:23][C:24]1[O:28][C:27]([C:29]([OH:31])=O)=[CH:26][C:25]=1[C:32]1[CH:37]=[CH:36][CH:35]=[C:34]([Cl:38])[CH:33]=1.C(N(CC)C(C)C)(C)C>>[Br:23][C:24]1[O:28][C:27]([C:29]([N:16]2[CH2:17][C:18](=[O:22])[NH:19][CH2:20]2)=[O:31])=[CH:26][C:25]=1[C:32]1[CH:37]=[CH:36][CH:35]=[C:34]([Cl:38])[CH:33]=1

참가 물질

4

반응물 3

HCID 81531DiisopropylethylamineHCID 580647644-{[4-Bromo-5-(3-chlorophenyl)furan-2-yl]carbonyl}piperazin-2-oneHCID 580648025-Bromo-4-(3-chlorophenyl)furan-2-carboxylic acid

생성물 1

HCID 580647691-{[5-Bromo-4-(3-chlorophenyl)furan-2-yl]carbonyl}imidazolidin-4-one

실험 절차

The preparation of the title compound takes place in analogy to the synthesis of the compound from Example 27A starting with the compound from Example 22A and the compound from Example 35A. 3.5 equivalents of N,N-diisopropylethylamine are used. During the reaction, the product precipitates. The precipitate is collected by suction filtration, washed with tetrahydrofuran and dried under high vacuum. 1.17 g (100% of theory) of the title compound are obtained.

후처리

  1. customDuring the reaction
  2. customthe product precipitates
  3. filtrationThe precipitate is collected by suction filtration
  4. washwashed with tetrahydrofuran
  5. customdried under high vacuum

출처 및 근거

ORD 기록
ord-704eba238ef14d22a5700948cafe02a1
출처 데이터셋
uspto-grants-2012_12
특허 번호
US08324268B2

반응 노트

불러오는 중…