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2-amino-N,N-dimethylacetamide hydrochloride → HCID 90375186, 화합물

HRID 1507141
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HRID 1507141 반응식
Cl.[CH3:2][N:3]([CH3:8])[C:4](=[O:7])[CH2:5][NH2:6].[Si:9]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][N:21]=[C:20]([CH:24]=O)[CH:19]=1)([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10]>C(N(CC)CC)C>[Si:9]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][N:21]=[C:20]([CH2:24][NH:6][CH2:5][C:4]([N:3]([CH3:8])[CH3:2])=[O:7])[CH:19]=1)([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:10])[CH3:11]
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참가 물질

4

반응물 2

HCID 201292832-amino-N,N-dimethylacetamide hydrochlorideHCID 90375103HCID 90375103, 화합물

생성물 1

HCID 90375186HCID 90375186, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

By General Procedure A from N,N-dimethylglycineamide hydrochloride, triethylamine, and 4-{[(tert-butyldimethylsilyl)oxy]methyl}pyridine-2-carbaldehyde. Purification by column chromatography (0-10% MeOH in DCM) gave the title product as yellow oil. 1H NMR (300 MHz, chloroform-d): δ ppm 8.49 (d, 1H), 7.32 (s, 1H), 7.17 (d, 1H), 4.74 (s, 2H), 3.97 (s, 2H), 3.47 (s, 2H), 2.95 (d, 6H), 0.95 (s, 9H), 0.11 (s, 6H).

후처리

  1. customPurification by column chromatography (0-10% MeOH in DCM)

출처 및 근거

ORD 기록
ord-be5c5211c1054de1974f7fbfa6db47ca
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221801B2

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