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N-methyldiaminoethylamine → HCID 178429407, 화합물

HRID 2038152
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반응식

HRID 2038152 반응식
[N:1]1([C:6]([NH:8][C:9]2[NH:10][C:11]([CH3:16])=[CH:12][C:13](=[O:15])[N:14]=2)=[O:7])[CH:5]=[CH:4][N:3]=[CH:2]1.[CH3:17][NH:18][CH2:19][CH:20](N)N>ClCCl>[CH3:2][N:3]([CH2:4][CH2:5][NH:1][C:6]([NH:8][C:17]1[NH:18][C:19]([CH3:20])=[CH:12][C:13](=[O:15])[N:14]=1)=[O:7])[CH2:4][CH2:5][NH:1][C:6]([NH:8][C:9]1[NH:10][C:11]([CH3:16])=[CH:12][C:13](=[O:15])[N:14]=1)=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 57077427N-methyldiaminoethylamineHCID 178429402HCID 178429402, 화합물

생성물 1

HCID 178429407HCID 178429407, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3 g of 2-(1-imidazolylcarbonylamino)-6-methyl-4[1H]-pyrimidinone (136 mmol) prepared according to the procedure described by Meijer et al., J. Am. Chem. Soc. 2003, 125, p. 6860 are added to a solution of 0.81 g of N-methyldiaminoethylamine (6.8 mmol) in 150 ml of dichloromethane. The solution is stirred at reflux for 4.5 hours. The product is precipitated from acetone, filtered off and washed with acetone, and then dried under reduced pressure.

후처리

  1. temperatureat reflux for 4.5 hours
  2. customThe product is precipitated from acetone
  3. filtrationfiltered off
  4. washwashed with acetone
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-f7e338553daf4af886cdecca32f74038
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08575341B2

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