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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrazine hydrate (1:1) → 6-(2-amino-indan-5-yl)-4,5-dihydropyridazin-3(2H)-one

HRID 1651853
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반응식

HRID 1651853 반응식
O.[NH2:2][NH2:3].Cl.[NH2:5][CH:6]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([C:15](=O)[CH2:16][CH2:17][C:18]([O:20]C)=O)[CH:12]=2)[CH2:7]1>C(O)(=O)C>[NH2:5][CH:6]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([C:15]3[CH2:16][CH2:17][C:18](=[O:20])[NH:2][N:3]=3)[CH:12]=2)[CH2:7]1
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참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 23050575Methyl 4-(2-amino-indan-5-yl)-4-oxobutyrate hydrochloride

생성물 1

HCID 140714996-(2-amino-indan-5-yl)-4,5-dihydropyridazin-3(2H)-one

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

8.5 g (0.17 mol) of 99% hydrazine hydrate are added to 10.0 g (0.035 mol) of methyl 4-(2-amino-indan-5-yl)-4-oxobutyrate hydrochloride in glacial acetic acid and the mixture is boiled for 30 minutes. The mixture is evaporated in vacuo, the residue is dissolved in water and the reaction product is precipitated by neutralisation with sodium hydroxide.

후처리

  1. customThe mixture is evaporated in vacuo
  2. dissolutionthe residue is dissolved in water
  3. customthe reaction product is precipitated by neutralisation with sodium hydroxide

출처 및 근거

ORD 기록
ord-ee1ae706f6be499fbb63e5d2423cc233
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04929754

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