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Sodium Hydroxide → N-benzyl-4-(benzylamino)-N'-hydroxy-1,2,5-oxadiazole-3-carboximidamide

HRID 82711
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인쇄 미리보기

반응식

HRID 82711 반응식
[CH2:1]([N:8]1C(=O)[O:11][N:10]=[C:9]1[C:14]1[C:18]([NH:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[N:17][O:16][N:15]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>C(O)C.O>[CH2:1]([NH:8][C:9]([C:14]1[C:18]([NH:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[N:17][O:16][N:15]=1)=[N:10][OH:11])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 58558319HCID 58558319, 화합물

생성물 1

HCID 178526382N-benzyl-4-(benzylamino)-N'-hydroxy-1,2,5-oxadiazole-3-carboximidamide수율 91%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

반응 조건

온도
25 °C

실험 절차

A solution of 4-benzyl-3-[4-(benzylamino)-1,2,5-oxadiazol-3-yl]-1,2,4-oxadiazol-5(4H)-one (12 mg, 34 μmol) in ethanol (1 mL) was treated with 2 M sodium hydroxide in water (300 μL) and stirred at 25° C. for 30 min. The reaction mixture was quenched with acetic acid and purified by preparative HPLC to give the desired product (10 mg, 90%) as a white solid. LCMS for C17H18N5O2 (M+H)+: m/z=324.2.

후처리

  1. customThe reaction mixture was quenched with acetic acid
  2. custompurified by preparative HPLC

출처 및 근거

ORD 기록
ord-30c9f702ca1e43abb259a527eadf0e3d
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846726B2

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