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4-Aminopyridine → 4-Pyridylcarbamoyl-beta-alanine ethyl ester

HRID 358555
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반응식

HRID 358555 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[N-:8]=[C:9]=[O:10].[CH2:11]([O:13][C:14](=[O:18])[CH2:15][CH2:16]N)[CH3:12]>C(#N)C>[CH2:11]([O:13][C:14](=[O:18])[CH2:15][CH2:16][NH:8][C:9](=[O:10])[NH:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1)[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 17274-AminopyridineHCID 86744639HCID 86744639, 화합물

생성물 1

HCID 200664534-Pyridylcarbamoyl-beta-alanine ethyl ester수율 99%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A solution of 1 g (10.64 mmol) of 4-aminopyridine and 2.3 g (15.9 mmol) of beta-alanine ethyl ester isocyanate in 30 ml of anhydrous acetonitrile is agitated for 20 hr at room temperature. After concentration to dryness and trituration of the resulting oily residue in ether (4 × 20 ml), 2.5 g (yield 88%) of 4-pyridylcarbamoyl-beta-alanine ethyl ester is obtained in the form of a solid having a melting point of 95° C.

후처리

  1. concentrationAfter concentration to dryness and trituration of the resulting oily residue in ether (4 × 20 ml)

출처 및 근거

ORD 기록
ord-87a00d5218a444b7b0b074f246b5a9f8
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04997667

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