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N1-tert-butylethane-1,2-diamine → HCID 14699565, 화합물

HRID 1608300
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인쇄 미리보기

반응식

HRID 1608300 반응식
[C:1]1([C:7]2[CH:8]=[N:9][N:10]([CH2:18][C:19](OCC)=[O:20])[C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:24][C:25]([NH:28][CH2:29][CH2:30][NH2:31])([CH3:27])[CH3:26]>C[O-].[Na+]>[CH3:24][C:25]([NH:28][CH2:29][CH2:30][NH:31][C:19](=[O:20])[CH2:18][N:10]1[C:11]([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:8]=[N:9]1)([CH3:27])[CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12504477N1-tert-butylethane-1,2-diamineHCID 146995514,5-Diphenyl-1-(ethoxycarbonylmethyl)-pyrazole

생성물 1

HCID 14699565HCID 14699565, 화합물수율 66.8%

시약·촉매·용매 1

HCID 10942334Sodium Methoxide촉매

실험 절차

A solution of 10.7 g (0.035 mol) of ethyl 4,5-diphenylpyrazole-1-acetate of example 1 in 10.9 g (0.094 mol) of 2-[(1,1-dimethylethyl)amino]ethanamine was heated with about 50 mg of sodium methoxide at about 150° for two hours. The excess amine was stripped off under vacuum and the residue was triturated in acetonitrile. The solid product was filtered off and recrystallized from isopropyl acetate to yield 8.8 g of white crystals, mp 115°-116° C.

후처리

  1. customthe residue was triturated in acetonitrile
  2. filtrationThe solid product was filtered off
  3. customrecrystallized from isopropyl acetate

출처 및 근거

ORD 기록
ord-c7d08bb897374f3093911c9283abbc83
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04870095

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