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1,4-Dioxane hydrochloride → HCID 178462643, 화합물

HRID 577008
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HRID 577008 반응식
[CH2:1]([N:3]1[CH:7]=[CH:6][N:5]=[C:4]1[CH2:8][S:9][C:10]1[N:15]=[C:14]([OH:16])[CH:13]=[C:12]([CH3:17])[N:11]=1)[CH3:2].[ClH:18].O1CCOCC1>CO>[ClH:18].[ClH:18].[CH2:1]([N:3]1[CH:7]=[CH:6][N:5]=[C:4]1[CH2:8][S:9][C:10]1[N:15]=[C:14]([OH:16])[CH:13]=[C:12]([CH3:17])[N:11]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 204431481,4-Dioxane hydrochlorideHCID 178462642HCID 178462642, 화합물

생성물 1

HCID 178462643HCID 178462643, 화합물수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture of 2-{[(1-ethyl-1H-imidazol-2-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol (215 mg, 0.86 mmol) in MeOH (3 mL) was added 4 M HCl/dioxane (2 mL, 8.0 mmol). The mixture became clear, and a solid precipitated. The solvent was evaporated. The solid product was dried in vacuo, affording the title compound (275 mg, 99% yield); 1H NMR (400 MHz, DMSO-d6): δ 1.38 (t, 3H, J=7.2 Hz), 2.16 (s, 3H), 4.29 (m, 2H), 4.73 (s, 2H), 6.17 (s, 1H), 7.61 (d, 1H, J=2.0 Hz), 7.15 (d, 1H, J=2.0 Hz); M+ 251.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customa solid precipitated
  2. customThe solvent was evaporated
  3. customThe solid product was dried in vacuo

출처 및 근거

ORD 기록
ord-d833275c729c435996aed7a53653de2e
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040538B2

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