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1,4-Dioxane hydrochloride → HCID 178462826, 화합물

HRID 630124
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HRID 630124 반응식
[CH2:1]([N:3]1[C:7]([CH3:8])=[C:6]([CH2:9][S:10][C:11]2[N:16]=[C:15]([OH:17])[CH:14]=[C:13]([CH3:18])[N:12]=2)[N:5]=[CH:4]1)[CH3:2].[ClH:19].O1CCOCC1>CO>[ClH:19].[CH2:1]([N:3]1[C:7]([CH3:8])=[C:6]([CH2:9][S:10][C:11]2[N:16]=[C:15]([OH:17])[CH:14]=[C:13]([CH3:18])[N:12]=2)[N:5]=[CH:4]1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 204431481,4-Dioxane hydrochlorideHCID 178462825HCID 178462825, 화합물

생성물 1

HCID 178462826HCID 178462826, 화합물수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture of 2-{[(1-ethyl-5-methyl-1H-imidazol-4-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol (60 mg, 0.23 mmol) in MeOH (2 mL) was added 4 M HCl/dioxane (500 μL, 2.0 mmol). The mixture was filtered to remove particles in suspension. The solution was evaporated and dried in vacuo, affording the title compound (68 mg, 99% yield); 1H NMR (400 MHz, DMSO-d6): δ 1.38 (t, 3H, J=6.7 Hz), 2.23 (s, 3H), 2.38 (s, 3H), 4.09 (m, 2H), 4.44 (s, 2H), 6.09 (s, 1H), 9.04 (s, 1H); M+266.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. filtrationThe mixture was filtered
  2. customto remove particles in suspension
  3. customThe solution was evaporated
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-df61981ea975459c90c061975daaaebb
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315521B2

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