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Tert-Butylamine → 1-(tert-Butylamino)-3-[2-(6-chloropyridazin-3-yl)phenoxy]propan-2-ol

HRID 1763237
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반응식

HRID 1763237 반응식
[Cl:1][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[O:14][CH2:15][CH:16]2[O:18][CH2:17]2)=[CH:6][CH:7]=1.[C:19]([NH2:23])([CH3:22])([CH3:21])[CH3:20]>CO>[Cl:1][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[O:14][CH2:15][CH:16]([OH:18])[CH2:17][NH:23][C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6385Tert-ButylamineHCID 13023013HCID 13023013, 화합물

생성물 1

HCID 30190301-(tert-Butylamino)-3-[2-(6-chloropyridazin-3-yl)phenoxy]propan-2-ol

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 3-chloro-6-(2-epoxypropoxyphenyl)pyridazine (0.7 g), methanol (7 ml) and t-butylamine (1.7 ml) was stirred and heated under reflux for 11/4 hours. The mixture was evaporated under reduced pressure at 50° and the residue was recrystallised from toluene to give the title product (1.28 g) m.p. 136.5°-137.5°.

후처리

  1. temperatureheated
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • temperatureunder reflux for 11/4 hours
  • customThe mixture was evaporated under reduced pressure at 50°
  • customthe residue was recrystallised from toluene
  • 출처 및 근거

    ORD 기록
    ord-545fc2ce118a4cd19a8cb5bf2be66a17
    출처 데이터셋
    uspto-grants-1978_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04111935

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