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Water → ethyl 8-bromo-2,2-dimethyl-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylate

HRID 1168507
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HRID 1168507 반응식
[CH3:1][C:2]1([CH3:20])[N:12]2[C:13]3[C:8]([C:9](=[O:19])[C:10]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:11]2)=[CH:7][CH:6]=[CH:5][C:4]=3[CH2:3]1.[Br:21]Br.O>C(O)(=O)C>[Br:21][C:6]1[CH:7]=[C:8]2[C:13]3=[C:4]([CH2:3][C:2]([CH3:1])([CH3:20])[N:12]3[CH:11]=[C:10]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:9]2=[O:19])[CH:5]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 24408BromineHCID 12083031HCID 12083031, 화합물

생성물 1

HCID 12083032ethyl 8-bromo-2,2-dimethyl-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylate수율 38%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Ethyl 2,2-dimethyl-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylate (Preparation 12, 1.03 g) is dissolved in acetic acid (10 mL) and bromine (213 μL) is added dropwise. The reaction is stirred an additional 30 min and then poured into water (50 mL). The resulting precipitate is filtered and then washed with ether to give 506 mg (38%) of the title compound as white crystals. Physical characteristics: M.p. 227-228° C.; 1H NMR (DMSO-d6) δ8.76, 7.90, 7.79, 4.23, 3.41, 1.63, 1.29; IR (diffuse reflectance) 1727, 1636, 1612, 1592, 1547, 1505, 1393, 1373, 1327, 1303, 1217, 1171, 1167, 1128, 804 cm−1; HRMS (FAB) 350.0386 (C16H16BrNO3+H).

후처리

  1. filtrationThe resulting precipitate is filtered
  2. washwashed with ether

출처 및 근거

ORD 기록
ord-c5bac66b8c1448fb87dd3bf4d669ec2a
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06624159B2

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