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(2-(Methylthio)ethyl)amine → HCID 90375166, 화합물

HRID 1507152
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HRID 1507152 반응식
[Si:1]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][N:13]=[C:12]([CH:16]=O)[CH:11]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[CH3:18][S:19][CH2:20][CH2:21][NH2:22]>>[Si:1]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][N:13]=[C:12]([CH2:16][NH:22][CH2:21][CH2:20][S:19][CH3:18])[CH:11]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 87697(2-(Methylthio)ethyl)amineHCID 90375103HCID 90375103, 화합물

생성물 1

HCID 90375166HCID 90375166, 화합물

실험 절차

By General Procedure A from 4-{[(tert-butyldimethylsilyl)oxy]methyl}pyridine-2-carbaldehyde and 2-(methylsulfanyl)ethan-1-amine. Purification by column chromatography (DCM/MeOH/NH4OH (90:10:1)) gave the title compound as yellow oil. 1H NMR (300 MHz, Methanol-d4): δ 8.4 (d, 1H), 7.3 (s, 1H), 7.1 (d, 1H), 4.7 (s, 2H), 3.9 (s, 2H), 2.7 (t, 2H), 2.6 (t, 2H), 2.58 (q, 2H), 1.2 (t, 3H), 0.9 (s, 9H).

후처리

  1. customPurification by column chromatography (DCM/MeOH/NH4OH (90:10:1))

출처 및 근거

ORD 기록
ord-41f633254a0049a3b669786264a64026
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
특허 번호
US09221801B2

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