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Water → Tert-butyl (6-iodoimidazo[1,2-b]pyridazin-2-yl)carbamate

HRID 1667802
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인쇄 미리보기

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HRID 1667802 반응식
[NH2:1][C:2]1[N:3]=[N:4][C:5]([I:8])=[CH:6][CH:7]=1.Cl[CH2:10][C:11]([NH:13][C:14](=[O:20])[O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=O.P([O-])([O-])(O)=O.[Na+].[Na+].O>CN(C)C(=O)C>[I:8][C:5]1[CH:6]=[CH:7][C:2]2[N:3]([CH:10]=[C:11]([NH:13][C:14](=[O:20])[O:15][C:16]([CH3:19])([CH3:18])[CH3:17])[N:1]=2)[N:4]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 24203Sodium Phosphate, DibasicHCID 108678346-Iodopyridazin-3-amineHCID 14221822tert-Butyl (2-chloroacetyl)carbamate

생성물 1

HCID 46941915Tert-butyl (6-iodoimidazo[1,2-b]pyridazin-2-yl)carbamate수율 63%

시약·촉매·용매 1

HCID 31374
Dimethylacetamide
용매

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온도
120 °C

실험 절차

To a solution of 3-amino-6-iodopyridazine (10.0 g, 45.2 mmol) in N,N-dimethylacetamide (100 mL) were added tert-butyl (chloroacetyl)carbamate (14.0 g, 72.4 mmol) and disodium hydrogenphosphate (16.1 g, 113 mmol), and the mixture was stirred at 120° C. for 3 hr. After cooling the mixture to room temperature, water (400 mL) was added to the mixture, and the precipitated crystals were filtrated, and washed with acetonitrile and petroleum ether to give the title compound (10.2 g, 63%) as a green powder.

후처리

  1. temperatureAfter cooling the mixture to room temperature
  2. filtrationthe precipitated crystals were filtrated
  3. washwashed with acetonitrile and petroleum ether

출처 및 근거

ORD 기록
ord-aa5d0997e61b4d249e11e4324f9a7d5e
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044049B2

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