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Acetone → HCID 178477737, 화합물

HRID 1665830
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HRID 1665830 반응식
[OH:1][NH:2][C:3](=[NH:32])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]3[N:24]=[C:25]([CH3:31])[S:26][C:27]=3[CH:28]([CH3:30])[CH3:29])=[CH:19][CH:18]=2)=[CH:6][CH:5]=1.[CH2:33]([S:35]([OH:38])(=[O:37])=[O:36])[CH3:34].CC(C)=O.CCCCCC>C(O)C>[CH3:34][CH2:33][S:35]([OH:38])(=[O:37])=[O:36].[OH:1][NH:2][C:3](=[NH:32])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]3[N:24]=[C:25]([CH3:31])[S:26][C:27]=3[CH:28]([CH3:29])[CH3:30])=[CH:19][CH:18]=2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 8058HexaneHCID 11668Ethanesulfonic acidHCID 178432563DW-1350

생성물 1

HCID 178477737HCID 178477737, 화합물수율 86%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

3 g (6.614 mmol) of N-hydroxy-4-{5-[4-(5-isopropyl-2-methyl-1,3-thiazol-4-yl)phenoxy]pentoxy}benzamidine was dissolved in 30 ml of ethanol, and was mixed with 1.14 ml (2.2 equivalents) of ethanesulfonic acid with agitation at room temperature for 1 hr. The solution was then mixed with 30 ml of acetone and 60 ml of hexane with agitation for 1 hr. The produced solid was recovered by filtration, washed with acetone, and dried under vacuum. As a result, 4.17 g (yield: 86%) of N-Hydroxy-4-{5-[4-(5-isopropyl-2-methyl-1,3-thiazol-4-yl)phenoxy]pentoxy}benzamidine 2 ethansulfonic acid salt was obtained as a white solid.

후처리

  1. filtrationThe produced solid was recovered by filtration
  2. washwashed with acetone
  3. customdried under vacuum

출처 및 근거

ORD 기록
ord-704ddf50658f40e9a3add45c8412c00b
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08039635B2

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