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Cesium carbonate → 4-(2-(4-(Benzo[D]thiazol-2-ylamino)phenoxy)pyridin-3-YL)cyclohexanol

HRID 1880105
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HRID 1880105 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[NH:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1.C(=O)([O-])[O-].[Cs+].[Cs+].F[C:25]1[C:30]([CH:31]2[CH2:36][CH2:35][CH:34]([OH:37])[CH2:33][CH2:32]2)=[CH:29][CH:28]=[CH:27][N:26]=1>CN1C(=O)CCC1.O>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[NH:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][C:25]2[C:30]([CH:31]3[CH2:32][CH2:33][CH:34]([OH:37])[CH2:35][CH2:36]3)=[CH:29][CH:28]=[CH:27][N:26]=2)=[CH:13][CH:12]=1
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참가 물질

6

반응물 3

HCID 10796Cesium carbonateHCID 585477094-(2-Fluoropyridin-3-yl)cyclohexanolHCID 593268134-(Benzo[d]thiazol-2-ylamino)phenol

생성물 1

HCID 593269514-(2-(4-(Benzo[D]thiazol-2-ylamino)phenoxy)pyridin-3-YL)cyclohexanol

시약·촉매·용매 2

HCID 962Water용매HCID 13387
N-methyl-2-pyrrolidone
용매

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온도
200 °C

실험 절차

To a vial containing 4-(benzo[d]thiazol-2-ylamino)phenol (819 mg, 3.38 mmol) was added cesium carbonate (918 mg, 2.82 mmol) followed by 4-(2-fluoropyridin-3-yl)cyclohexanol (220 mg, 1.127 mmol) as a solution in NMP (7.5 mL). The reaction mixture was heated to 200° C. for 2.5 h with microwave irradiation. The reaction mixture was diluted with water and extracted with 15% IPA:chloroform before drying over magnesium sulfate, filtering, and concentrating to a dark brown residue under reduced pressure.

후처리

  1. extractionextracted with 15% IPA
  2. dry with materialchloroform before drying over magnesium sulfate
  3. filtrationfiltering
  4. concentrationconcentrating to a dark brown residue under reduced pressure

출처 및 근거

ORD 기록
ord-d0c56bd6641e4cfb825bb057e4651d36
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318718B2

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