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Diisopropylethylamine → HCID 23121832, 화합물

HRID 1713549
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HRID 1713549 반응식
[NH2:1][C:2]1[C:10]2[N:9]=[CH:8][N:7]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[C:6]=2[CH:5]=[CH:4][CH:3]=1.C(N(C(C)C)CC)(C)C.Cl[C:28](OC1C=CC([N+]([O-])=O)=CC=1)=[O:29].[C:40]1([C:46]2([C:56]3[CH:61]=[CH:60][CH:59]=[CH:58][CH:57]=3)[CH:50]3[CH2:51][NH:52][CH2:53][CH2:54][N:49]3[C:48](=[O:55])[O:47]2)[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1>O1CCCC1.C(OCC)(=O)C>[O:55]=[C:48]1[N:49]2[CH2:54][CH2:53][N:52]([C:28]([NH:1][C:2]3[C:10]4[N:9]=[CH:8][N:7]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[C:6]=4[CH:5]=[CH:4][CH:3]=3)=[O:29])[CH2:51][CH:50]2[C:46]([C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)([C:56]2[CH:57]=[CH:58][CH:59]=[CH:60][CH:61]=2)[O:47]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 81531Diisopropylethylamine2회HCID 821294-Nitrophenyl chloroformateHCID 18355224tert-butyl 4-amino-1H-benzo[d]imidazole-1-carboxylateHCID 231218811,1-Diphenyltetrahydro-1H-oxazolo[3,4-a]pyrazin-3(5H)-one

생성물 1

HCID 23121832HCID 23121832, 화합물수율 66.2%

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 1,1-dimethylethyl 4-amino-1H-benzimidazole-1-carboxylate (0.12 g, 0.50 mmol) in tetrahydrofuran (10 ml) were added diisopropylethylamine (90 μL, 0.50 mmol) and 4-nitrophenyl chloroformate (0.11 g, 0.50 mmol), and the mixture was stirred at room temperature for 4 hours. Hexahydro-1,1-diphenyl-3H-oxazolo[3,4-a]pyrazin-3-one (88 mg, 0.30 mmol) and diisopropylethylamine (90 μL, 0.50 mmol) were sequentially added thereto, and the mixture was stirred at room temperature overnight. To the reaction solution were added ethyl acetate (50 mL) and a 0.5 M aqueous sodium hydrogen carbonate solution (50 mL), and the obtained crystals were collected by filtration. The crude crystals were sequentially washed with a 0.5 M aqueous sodium hydrogen carbonate solution, water and ethyl acetate to obtain the title compound (0.11 g, yield 65%).

후처리

  1. stirringthe mixture was stirred at room temperature overnight
  2. filtrationa 0.5 M aqueous sodium hydrogen carbonate solution (50 mL), and the obtained crystals were collected by filtration
  3. washThe crude crystals were sequentially washed with a 0.5 M aqueous sodium hydrogen carbonate solution, water and ethyl acetate

출처 및 근거

ORD 기록
ord-e96e984172474199a9b694d2934f0013
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07795267B2

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