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tert-Butoxy bis(dimethylamino)methane → HCID 69219756, 화합물

HRID 271098
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인쇄 미리보기

반응식

HRID 271098 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[CH2:14][C:15](=[O:18])[NH:16][N:17]=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].C(O[CH:24](N(C)C)[N:25]([CH3:27])[CH3:26])(C)(C)C>C(#N)C>[CH3:24][N:25]([CH:27]=[C:14]1[C:13]([C:5]2[CH:6]=[C:7]([O:11][CH3:12])[C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=2)=[N:17][NH:16][C:15]1=[O:18])[CH3:26]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 79885tert-Butoxy bis(dimethylamino)methaneHCID 22353179HCID 22353179, 화합물

생성물 1

HCID 69219756HCID 69219756, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
35 °C

실험 절차

5-(3,4,5-Trimethoxyphenyl)-2,4-dihydro-pyrazol-3-one (k, 2 g) in dry actonitrile (10 mL) was added C-tert-Butoxy-N,N,N′,N′-tetramethyl-methanediamine (3 mL) and stirred at 35° C. The reaction was monitored by HPLC. After 36 hours, the solid was filtered and rinsed with dry acetonitrile (5 mL) and dried under nitrogen pressure to yield the title compound (l).

후처리

  1. filtrationthe solid was filtered
  2. washrinsed with dry acetonitrile (5 mL)
  3. customdried under nitrogen pressure

출처 및 근거

ORD 기록
ord-1bacf2bd0e1e487383478c503b725d37
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452873B2

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