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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 6-Chloro-3-chloromethyl-4-methoxypyridazine

HRID 1244249
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HRID 1244249 반응식
O=S(Cl)[Cl:3].[Cl:5][C:6]1[N:11]=[N:10][C:9]([CH2:12]O)=[C:8]([O:14][CH3:15])[CH:7]=1>C(Cl)Cl>[Cl:5][C:6]1[N:11]=[N:10][C:9]([CH2:12][Cl:3])=[C:8]([O:14][CH3:15])[CH:7]=1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 21919279(6-Chloro-4-methoxypyridazin-3-YL)methanol

생성물 1

HCID 219192946-Chloro-3-chloromethyl-4-methoxypyridazine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Excess SOCl2 is added to a stirred solution of (6-chloro-4-methoxy-pyridazin-3-yl)-methanol (140 mg, 0.8 mmol) in CH2Cl2 (4 mL). The reaction mixture is stirred at room temperature for 4 hours. The solvent is removed in vacuo; toluene (4 mL) is added and evaporated to dryness. Flash column chromatography (silica gel) purification of the residue provides 6-chloro-3-chloromethyl-4-methoxy-pyridazine as a clear oil.

후처리

  1. customThe solvent is removed in vacuo
  2. additiontoluene (4 mL) is added
  3. customevaporated to dryness
  4. customFlash column chromatography (silica gel) purification of the residue

출처 및 근거

ORD 기록
ord-7dc2075a0418446cb3fd2714965154c1
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07122546B2

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