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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tyramine → 4-[2-(4-Chloro-pyrimidin-2-ylamino)-ethyl]-phenol

HRID 14834
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인쇄 미리보기

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HRID 14834 반응식
Cl[C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[CH:4][N:3]=1.[NH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][CH:13]=1>CN(C=O)C>[Cl:8][C:6]1[CH:5]=[CH:4][N:3]=[C:2]([NH:9][CH2:10][CH2:11][C:12]2[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][CH:13]=2)[N:7]=1
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참가 물질

4

반응물 2

HCID 5610TyramineHCID 775312,4-Dichloropyrimidine

생성물 1

HCID 866032814-[2-(4-Chloro-pyrimidin-2-ylamino)-ethyl]-phenol수율 15%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2,4 dichloropyrimidine (1.49 g) was dissolved in DMF along with diisopropylethylmine (1.29 g) and tyramine (1.37 g.) The mixture was stirred at room temperature overnight. The mixture was partitioned between ethyl acetate and water and the organic layer washed with 1 N HCl followed by saturated NaHCO3 and brine. The solvent was removed and the residue subjected to flash chromatography (ethyl acetate as eluent.) 4-[2-(4-Chloro-pyrimidin-2-ylamino)-ethyl]-phenol eluted first and was isolate as a minor product (15% yield.) LC-MS showed the product had the expected M+H+ of 250.

후처리

  1. customThe mixture was partitioned between ethyl acetate and water
  2. washthe organic layer washed with 1 N HCl
  3. customThe solvent was removed
  4. customwas isolate as a minor product (15% yield.) LC-MS

출처 및 근거

ORD 기록
ord-cb753924c8904dcc99670ddcaa26658b
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732444B2

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