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

HRID 895356
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인쇄 미리보기

반응식

HRID 895356 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 (1).

후처리

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

출처 및 근거

ORD 기록
ord-d8b6203e262f447c99ff3e29c4b90476
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06916798B2

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