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Chlorosuccinimide → 3-Chloro-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

HRID 1831917
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인쇄 미리보기

반응식

HRID 1831917 반응식
[F:1][C:2]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:3]=1[CH2:4][O:5][C:6]1[CH:11]=[CH:10][NH:9][C:8](=[O:12])[CH:7]=1.[Cl:18]N1C(=O)CCC1=O>CC(O)=O>[Cl:18][C:7]1[C:8](=[O:12])[NH:9][CH:10]=[CH:11][C:6]=1[O:5][CH2:4][C:3]1[CH:13]=[CH:14][C:15]([F:17])=[CH:16][C:2]=1[F:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 220503904-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

생성물 1

HCID 220499783-Chloro-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a solution of 4-[(4-fluorobenzyl)oxy]pyridine-2(1H)-one (from Step 2, Example 74) (1.4 g, 5.9 mmol) in AcOH (25 mL) was added N-chlorosuccinimide (0.95 g, 7.1 mmol) and the reaction mixture was heated at reflux for 2 h. The solvent was removed under reduced pressure. 1H NMR (300 MHz, MeOD) δ 7.63-7.55 (m, 1H), 7.45 (d, J=8 Hz, 1H), 7.07-7.00 (m, 2H), 6.58 (d, J=8 Hz, 1H), 5.31 (d, J=8 Hz, 1H).

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 2 h
  3. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-552bc6639db94652a5f79349603f0f6c
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067540B2

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