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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → N-(3-bromopropyl)-2,6-dichloropyrimidin-4-amine

HRID 920360
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HRID 920360 반응식
[Cl:1][C:2]1[N:7]=[C:6](Cl)[CH:5]=[C:4]([Cl:9])[N:3]=1.C(N(CC)CC)C.Br.[Br:18][CH2:19][CH2:20][CH2:21][NH2:22]>C(#N)C>[Br:18][CH2:19][CH2:20][CH2:21][NH:22][C:6]1[CH:5]=[C:4]([Cl:9])[N:3]=[C:2]([Cl:1])[N:7]=1
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 773782,4,6-TrichloropyrimidineHCID 787013-Bromopropylamine hydrobromide

생성물 1

HCID 86676391N-(3-bromopropyl)-2,6-dichloropyrimidin-4-amine수율 30.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A solution of 2,4,6-trichloropyrimidine (100 g, 545 mmol) in acetonitrile (2000 mL) was added triethylamine (166 g, 1636 mmol) at 0° C., The reaction mixture was stirred for 5 min at rt, then 3-bromopropan-1-amine hydrobromide (119 g, 545 mmol) was added portionwise. The reaction mixture was stirred for 1 h at rt, and filtered to provide a clear solution. Purification via FC afforded the title compound as a white solid (47 g, 30% yield).

후처리

  1. stirringThe reaction mixture was stirred for 1 h at rt
  2. filtrationfiltered
  3. customto provide a clear solution
  4. customPurification via FC

출처 및 근거

ORD 기록
ord-4e833e5c2c734f7eafcbd68c19c51199
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273054B2

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