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2-(Bromomethyl)tetrahydro-2H-pyran → Ammonium Hydroxide

HRID 1470007
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인쇄 미리보기

반응식

HRID 1470007 반응식
[NH2:1][C:2]1[S:3][C:4]([CH3:7])=[CH:5][N:6]=1.Br[CH2:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][O:11]1>>[NH4+:1].[OH-:11].[CH3:7][C:4]1[S:3][C:2](=[NH:1])[N:6]([CH2:9][CH:10]2[CH2:15][CH2:14][CH2:13][CH2:12][O:11]2)[CH:5]=1
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참가 물질

4

반응물 2

HCID 1419172-(Bromomethyl)tetrahydro-2H-pyranHCID 3517702-Amino-5-methylthiazole

생성물 2

HCID 14923Ammonium HydroxideHCID 668596105-Methyl-3-(tetrahydro-pyran-2-ylmethyl)-3H-thiazol-2-ylideneamine

반응 조건

온도
85 °C

실험 절차

A mixture of 2-amino-5-methylthiazole (1.2 g, 11 mmol) and 2-(bromomethyl)tetrahydro-2H-pyran (1.5 mL, 12 mmol) was warmed to 85° C. and stirred for 18 hours. The mixture was cooled to ambient temperature and purified via flash column chromatography (SiO2, 10% methanol in ethyl acetate then 9:1:0.1 CH2Cl2:methanol:NH4OH) to afford the title compound. MS (DCI/NH3) m/z 213 (M+H)+.

후처리

  1. temperatureThe mixture was cooled to ambient temperature
  2. custompurified via flash column chromatography (SiO2, 10% methanol in ethyl acetate

출처 및 근거

ORD 기록
ord-ac4974e7146346dda5c8dbd0ddc1de22
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006275B2

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