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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hexamethylenetetramine → 1-[2-(3,5-Dichloropyridin-2-yl)-2-oxoethyl]-1,3,5,7-tetraazatricyclo[3,3,1,13,7]decan-1-ium bromide

HRID 56008
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HRID 56008 반응식
[Br:1][CH2:2][C:3]([C:5]1[C:10]([Cl:11])=[CH:9][C:8]([Cl:12])=[CH:7][N:6]=1)=[O:4].[N:13]12[CH2:22][N:17]3[CH2:18][N:19]([CH2:21][N:15]([CH2:16]3)[CH2:14]1)[CH2:20]2>C(Cl)(Cl)Cl>[Br-:1].[Cl:11][C:10]1[C:5]([C:3](=[O:4])[CH2:2][N+:13]23[CH2:22][N:17]4[CH2:18][N:19]([CH2:21][N:15]([CH2:16]4)[CH2:14]2)[CH2:20]3)=[N:6][CH:7]=[C:8]([Cl:12])[CH:9]=1
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참가 물질

4

반응물 2

HCID 4101HexamethylenetetramineHCID 534166072-Bromo-1-(3,5-dichloropyridin-2-yl)ethanone

생성물 1

HCID 1180716121-[2-(3,5-Dichloropyridin-2-yl)-2-oxoethyl]-1,3,5,7-tetraazatricyclo[3,3,1,13,7]decan-1-ium bromide수율 97.3%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

5.00 g of the 2-bromo-1-(3,5-dichloropyridin-2-yl)ethanone prepared in Step 2 in Synthetic Example 2 in 30 ml of chloroform was added dropwise to 2.61 g of 1,3,5,7-tetraazatricyclo[3,3,1,13,7]decane in 50 ml of chloroform with stirring at room temperature, and the mixture was stirred at the same temperature for 2 hours. After completion of the reaction, the precipitated crystals were collected by filtration and washed with 30 ml of chloroform to obtain 7.40 g of the desired product as white crystals.

후처리

  1. stirringthe mixture was stirred at the same temperature for 2 hours
  2. customAfter completion of the reaction
  3. filtrationthe precipitated crystals were collected by filtration
  4. washwashed with 30 ml of chloroform

출처 및 근거

ORD 기록
ord-0e9acf13518646259019b6accebbd0fd
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434684B2

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