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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Chlorine → Methyl-6-amino-5-chloro-2-methoxypyridine-3-carboxylate

HRID 1939245
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HRID 1939245 반응식
[CH3:1][O:2][C:3]([C:5]1[C:6]([O:12][CH3:13])=[N:7][C:8]([NH2:11])=[CH:9][CH:10]=1)=[O:4].[Cl:14]Cl>C(O)(=O)C>[CH3:1][O:2][C:3]([C:5]1[C:6]([O:12][CH3:13])=[N:7][C:8]([NH2:11])=[C:9]([Cl:14])[CH:10]=1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24526ChlorineHCID 11159681Methyl 6-amino-2-methoxynicotinate

생성물 1

HCID 22101798Methyl-6-amino-5-chloro-2-methoxypyridine-3-carboxylate수율 67.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

A solution of methyl-6-amino-2-methoxypyridine-3-carboxylate (0.4 g) in acetic acid (10 ml) was treated with a solution of Cl2 (0.19 g) in HOAc (4 ml) at room temperature for 3 h. The AcOH was removed by rotary evaporation and the residue treated with aqueous NaHCO3 (50 mL) and the product extracted into EtOAc (100 mL). Evaporation afforded methyl-6-amino-5-chloro-2-methoxypyridine-3-carboxylate (0.32 g).

후처리

  1. customThe AcOH was removed by rotary evaporation
  2. additionthe residue treated with aqueous NaHCO3 (50 mL)
  3. extractionthe product extracted into EtOAc (100 mL)
  4. customEvaporation

출처 및 근거

ORD 기록
ord-8ee492bec8e14475aa6f0e1f353636af
출처 데이터셋
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05696129

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