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Morpholine → 4-Chloro-2-morpholin-4-yl-1,3-thiazole-5-carbonitrile

HRID 2091699
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HRID 2091699 반응식
Cl[C:2]1[S:3][C:4]([C:8]#[N:9])=[C:5]([Cl:7])[N:6]=1.C(N(CC)C(C)C)(C)C.[NH:19]1[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1>C(O)C.O>[Cl:7][C:5]1[N:6]=[C:2]([N:19]2[CH2:24][CH2:23][O:22][CH2:21][CH2:20]2)[S:3][C:4]=1[C:8]#[N:9]
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참가 물질

6

반응물 3

HCID 8083MorpholineHCID 81531DiisopropylethylamineHCID 155763592,4-Dichloro-5-cyanothiazole

생성물 1

HCID 592500134-Chloro-2-morpholin-4-yl-1,3-thiazole-5-carbonitrile수율 95.9%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

2,4-dichloro-5-cyanothiazole (1.26 g, 0.00704 mol) and N,N-diisopropylethylamine (3.68 mL, 0.0211 mol) were dissolved in ethanol at 70° C. Morpholine (0.614 mL, 0.0704 mol) was added to the hot solution and the mixture was stirred for 30 minutes, cooled down to rt, diluted with water (50 mL) and the formed precipitate was collected to give the title compound (1.55 g, 91%). LCMS: (FA) ES+, 230. 1H NMR (300 MHz, d6-DMSO) δ: 3.71-3.67 (m, 4H), 3.52-3.48 (m, 4H).

후처리

  1. customthe formed precipitate was collected

출처 및 근거

ORD 기록
ord-535d736ad8034887aadbb81912ba3c02
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08440664B2

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