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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N,O-Dimethylhydroxylamine → 6-Chloro-pyrimidine-4-carboxylic acidmethoxy-methyl-amide

HRID 469300
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인쇄 미리보기

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HRID 469300 반응식
CCN(C(C)C)C(C)C.[Cl:10][C:11]1[N:16]=[CH:15][N:14]=[C:13]([C:17](Cl)=[O:18])[CH:12]=1.[CH3:20][NH:21][O:22][CH3:23]>C(Cl)Cl>[CH3:23][O:22][N:21]([CH3:20])[C:17]([C:13]1[CH:12]=[C:11]([Cl:10])[N:16]=[CH:15][N:14]=1)=[O:18]
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참가 물질

5

반응물 3

HCID 14232N,O-DimethylhydroxylamineHCID 81531DiisopropylethylamineHCID 184220986-Chloropyrimidine-4-carbonyl chloride

생성물 1

HCID 581812166-Chloro-pyrimidine-4-carboxylic acidmethoxy-methyl-amide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

반응 조건

온도
0 °C

실험 절차

20.7 mL (0.120 mol) DIPEA were added at 0° C. to 10.7 g (54.4 mmol) 6-chloropyrimidine-4-carboxylic acid chloride and 5.50 g (56.4 mmol) N,O-dimethylhydroxylamine in 150 mL DCM and stirred for 1 h at 0° C. and 1 h at RT. The mixture was diluted with DCM and washed with water. The organic phase was dried on sodium sulphate, filtered and evaporated down.

후처리

  1. washwashed with water
  2. customThe organic phase was dried on sodium sulphate
  3. filtrationfiltered
  4. customevaporated down

출처 및 근거

ORD 기록
ord-8b437771f8824af9836eb3de4a1f57ee
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08629137B2

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