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Lithium iodide → HCID 66685610, 화합물

HRID 1778400
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HRID 1778400 반응식
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[S:9]([NH:12][C:13]1[C:22]([C:23]([O:25]C)=[O:24])=[C:21]2[C:16]([C:17]3[CH:30]=[CH:29][O:28][C:18]=3[C:19](=[O:27])[NH:20]2)=[CH:15][CH:14]=1)(=[O:11])=[O:10].[I-].[Li+]>N1C=CC=CC=1>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[S:9]([NH:12][C:13]1[C:22]([C:23]([OH:25])=[O:24])=[C:21]2[C:16]([C:17]3[CH:30]=[CH:29][O:28][C:18]=3[C:19](=[O:27])[NH:20]2)=[CH:15][CH:14]=1)(=[O:11])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 66321Lithium iodideHCID 66685239HCID 66685239, 화합물2회

생성물 1

HCID 66685610HCID 66685610, 화합물수율 88.9%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A mixture of methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydrofuro[2,3-c]quinoline-6-carboxylate (Intermediate 87, 0.220 g) and lithium iodide (0.055 g) in pyridine (13 mL) was irradiated in the microwave at 150° C. for 30 minutes. After cooling, the mixture was concentrated in vacuo and the residue was suspended in 1M HCl. The solid was collected by filtration and triturated with acetone then dried under vacuum to give 7-(2-bromo-4-fluorobenzenesulfonylamino)-4-oxo-4,5-dihydro furo[2,3-c]quinoline-6-carboxylic acid (0.190 g) as a grey solid.

후처리

  1. customwas irradiated in the microwave at 150° C. for 30 minutes
  2. temperatureAfter cooling
  3. concentrationthe mixture was concentrated in vacuo
  4. filtrationThe solid was collected by filtration
  5. customtriturated with acetone
  6. customthen dried under vacuum

출처 및 근거

ORD 기록
ord-a7969ea3625c45e5882e73b0b2c26595
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09266896B2

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