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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → Methyl 4-amino-5,6-dichloropicolinate

HRID 2407808
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인쇄 미리보기

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HRID 2407808 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([C:9]([O:11][CH3:12])=[O:10])[CH:3]=1.[Cl:13]N1C(=O)CCC1=O.C(=O)(O)[O-].[Na+].O>CN(C)C=O>[NH2:1][C:2]1[C:7]([Cl:13])=[C:6]([Cl:8])[N:5]=[C:4]([C:9]([O:11][CH3:12])=[O:10])[CH:3]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 31398ChlorosuccinimideHCID 516892Sodium BicarbonateHCID 53485174Methyl 4-amino-6-chloropyridine-2-carboxylate

생성물 1

HCID 58504072Methyl 4-amino-5,6-dichloropicolinate수율 66%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
50 °C

실험 절차

The compound prepared in Example 404 (3.120 g) and N-chlorosuccinimide (2.456 g) were suspended in dimethyl formamide (100 mL) and stirred at 50° C. overnight. The reaction mixture was heated at 70° C. for a further 3 hours. The reaction mixture was added drop-wise to a stirred solution of 1:1 saturated aqueous sodium bicarbonate and water. The slurry was filtered and the solids dried under high vacuum to furnish the title compound (2.438 g), possessing the following physical data.

후처리

  1. temperatureThe reaction mixture was heated at 70° C. for a further 3 hours
  2. filtrationThe slurry was filtered
  3. customthe solids dried under high vacuum

출처 및 근거

ORD 기록
ord-93104871107f402da7d82396c220118d
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08809538B2

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