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Hydrochloric Acid → HCID 178493485, 화합물

HRID 2207084
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HRID 2207084 반응식
[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([OH:9])[C:6]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH2:19][CH2:20][O:21][Si](C(C)(C)C)(C)C)=[CH:13][C:12]=2[O:29][CH3:30])=[C:5]([CH3:31])[N:4]=1>CO>[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([OH:9])[C:6]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH2:19][CH2:20][OH:21])=[CH:13][C:12]=2[O:29][CH3:30])=[C:5]([CH3:31])[N:4]=1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 1784934872-amino-5-[[4-[3-[tert-butyl(dimethyl)silyl]oxypropoxy]-2-methoxyphenyl]methyl]-6-methyl-1H-pyrimidin-4-one

생성물 1

HCID 178493485HCID 178493485, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Concentrated hydrogen chloride (2.5 mL) was added dropwise to a solution of the product from step (v) (4.33 g) in methanol (43 mL) at RT and stirred for 14 h. The mixture was concentrated and diluted with methanol. The precipitate was collected by filtration, washed with methanol and dried to give 2.87 g of the sub-title compound as a white solid, which was used without further purification; 1H NMR (300 MHz, d6-DMSO) δ=12.59 (2H, brs), 8.05 (2H, s), 6.89 (1H, d), 6.51 (1H, d), 6.36 (1H, dd), 3.97 (2H, t), 3.52 (2H, t), 3.46 (2H, s), 2.13 (3H, s), 1.78-1.86 (2H, m); LC-MS: m/z 320.

후처리

  1. concentrationThe mixture was concentrated
  2. additiondiluted with methanol
  3. filtrationThe precipitate was collected by filtration
  4. washwashed with methanol
  5. customdried

출처 및 근거

ORD 기록
ord-0281b9c3933f4eb6a927d9594ff5ff6c
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09376398B2

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