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Hydrochloric Acid → 2-amino-5H,6H,7H-cyclopenta[b]pyridine-3-carboxylic acid

HRID 2079981
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반응식

HRID 2079981 반응식
C([O:3][C:4]([C:6]1[CH:7]=[C:8]2[CH2:15][CH2:14][CH2:13][C:9]2=[N:10][C:11]=1[NH2:12])=[O:5])C.[OH-].[Na+].Cl>C(O)C>[NH2:12][C:11]1[N:10]=[C:9]2[CH2:13][CH2:14][CH2:15][C:8]2=[CH:7][C:6]=1[C:4]([OH:5])=[O:3]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 13194076HCID 13194076, 화합물

생성물 1

HCID 545950242-amino-5H,6H,7H-cyclopenta[b]pyridine-3-carboxylic acid수율 83%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
100 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

2-Amino-6,7-dihydro-5H-cyclopenta[b]pyridine-3-carboxylic acid ethyl ester (0.2 g, 0.97 mmol) described in Preparation Example C-4 was dissolved in ethanol (15 mL), an aqueous solution of 1N sodium hydroxide (7.5 mL) was added thereto, followed by heating at 100° C. for 30 minutes. The reaction solution was allowed to room temperature, then cooled on an ice bath, and neutralized with 1N hydrochloric acid. The precipitated solid was collected by filtration, rinsed with water, then dried, and the title compound (143 mg, 0.8 mmol, 83%) was obtained.

후처리

  1. customwas allowed to room temperature
  2. temperaturecooled on an ice bath
  3. filtrationThe precipitated solid was collected by filtration
  4. washrinsed with water
  5. customdried

출처 및 근거

ORD 기록
ord-bff47f3cb618418083a0dddb84e88deb
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932272B2

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