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Ethyl 2-formylpyridine-4-carboxylate → HCID 90375097, 화합물

HRID 1507139
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인쇄 미리보기

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HRID 1507139 반응식
[CH:1]([C:3]1[CH:8]=[C:7]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:6]=[CH:5][N:4]=1)=O.Cl.[CH3:15][N:16]([CH3:21])[C:17](=[O:20])[CH2:18][NH2:19]>C(N(CC)CC)C>[CH3:15][N:16]([CH3:21])[C:17]([CH2:18][NH:19][CH2:1][C:3]1[CH:8]=[C:7]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:6]=[CH:5][N:4]=1)=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 19600808Ethyl 2-formylpyridine-4-carboxylateHCID 20129283N,N-Dimethylglycinamide--hydrogen chloride (1/1)

생성물 1

HCID 90375097HCID 90375097, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

By General Procedure A from Ethyl 2-formylpyridine-4-carboxylate, N,N-dimethylglycineamide hydrochloride, and triethylamine. Purification by column chromatography with a gradient of 0-10% MeOH in DCM gave the title product as yellow oil. 1H NMR (300 MHz, chloroform-d): δ ppm 8.69 (s, 1H), 7.94 (s, 1H), 7.72 (d, 1H), 4.40 (q, 2H), 4.03 (s, 2H), 3.48 (s, 2H), 2.95 (d, 6H), 1.40 (t, 3H).

후처리

  1. customPurification by column chromatography with a gradient of 0-10% MeOH in DCM

출처 및 근거

ORD 기록
ord-bdf493bce85e4bf5aab0eef62da8dbb2
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221801B2

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