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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Glycine → (3-Nitro-pyridin-2-ylamino)-acetic acid

HRID 881046
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인쇄 미리보기

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HRID 881046 반응식
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].[NH2:17][CH2:18][C:19]([OH:21])=[O:20]>CCO.O>[N+:8]([C:7]1[C:2]([NH:17][CH2:18][C:19]([OH:21])=[O:20])=[N:3][CH:4]=[CH:5][CH:6]=1)([O-:10])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 750GlycineHCID 11430Potassium CarbonateHCID 796132-Chloro-3-nitropyridine

생성물 1

HCID 3722651(3-Nitro-pyridin-2-ylamino)-acetic acid

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

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온도
0 °C

실험 절차

2-Chloro-3-nitropyridine (5 g, 31.5 mmol) was dissolved in EtOH (125 ml), added potassium carbonate (4.35 g, 31.5 mmol) and to this mixture glycine (4.73 g, 6.3 mmol) in 25 ml water was added and refluxed for overnight. The reaction mixture cooled to 0° C. to obtain the solid. Then EtOH was removed on rotavapour and acidified with 2N HCl and solid filtered and dried on vacuum to obtain the title compound quantitatively as a yellow solid.

후처리

  1. temperaturerefluxed for overnight
  2. customto obtain the solid
  3. customThen EtOH was removed on rotavapour
  4. filtrationfiltered
  5. customdried on vacuum

출처 및 근거

ORD 기록
ord-7c5f66d7d2eb4c84a09dd6c8c4b16539
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993612B2

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