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Cesium carbonate → 1-(6-Bromobenzo[d]thiazol-2-yl)azetidin-3-ol

HRID 1691972
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HRID 1691972 반응식
Br[C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]([N:12]1[CH2:15][CH:14]([OH:16])[CH2:13]1)=[S:11].C([O-])([O-])=O.[Cs+].[Cs+]>C(#N)C>[Br:8][C:6]1[CH:5]=[CH:4][C:3]2[N:9]=[C:10]([N:12]3[CH2:15][CH:14]([OH:16])[CH2:13]3)[S:11][C:2]=2[CH:7]=1
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참가 물질

4

반응물 2

HCID 10796Cesium carbonateHCID 86631905N-(2,4-dibromophenyl)-3-hydroxyazetidine-1-carbothioamide

생성물 1

HCID 669060671-(6-Bromobenzo[d]thiazol-2-yl)azetidin-3-ol

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
150 °C

실험 절차

N-(2,4-Dibromophenyl)-3-hydroxyazetidine-1-carbothioamide (0.366 g, 1.0 mmol) and Cs2CO3 (0.489 g, 1.5 mmol) were suspended in acetonitrile (10 mL), and the stirred reaction mixture was heated under microwave irradiation at 150° C. for 12 minutes. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (2:1 to 1:2 hexane/ethyl acetate) to provide 1-(6-bromobenzo[d]thiazol-2-yl)azetidin-3-ol. 1H NMR (300 MHz, DMSO-d6) δ ppm 3.85-3.91 (m, 2H), 4.29-4.36 (m, 2H), 4.61-4.72 (m, 1H), 5.90 (d, J=8 Hz, 1H), 7.36-7.44 (m, 2H), 8.02-8.03 (m, 1H); MS (DCI/NH3) m/z 285 (M+H)+.

후처리

  1. customthe stirred reaction mixture
  2. filtrationThe reaction mixture was filtered
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe resulting residue was purified by silica gel chromatography (2:1 to 1:2 hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-917224ee00b04dbb80b7d0afc8694c28
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153813B2

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