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Ethyl orthoformate → 4-Chloro-7-cyclopropyl-7H-imidazo[4,5-c]pyridazine

HRID 1846056
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HRID 1846056 반응식
[Cl:1][C:2]1[C:3]([NH2:12])=[C:4]([NH:8][CH:9]2[CH2:11][CH2:10]2)[N:5]=[N:6][CH:7]=1.[CH2:13](OC(OCC)OCC)C>>[Cl:1][C:2]1[C:3]2[N:12]=[CH:13][N:8]([CH:9]3[CH2:10][CH2:11]3)[C:4]=2[N:5]=[N:6][CH:7]=1
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참가 물질

3

반응물 2

HCID 31214Ethyl orthoformateHCID 867232775-Chloro-N3-cyclopropylpyridazine-3,4-diamine

생성물 1

HCID 867232784-Chloro-7-cyclopropyl-7H-imidazo[4,5-c]pyridazine수율 48%

실험 절차

A mixture of 5-chloro-N-3-cyclopropylpyridazine-3,4-diamine (Preparation 90, 10.0 g, 54 mmol) and triethylorthoformate (120 mL) were heated to reflux for 3 hours. The reaction mixture was concentrated in vacuo and the residue was purified by silica gel column chromatography eluting with CH2Cl2:MeOH 98:2 to afford the title compound as a brown solid in 48% yield, 5 g.

후처리

  1. temperaturewere heated
  2. temperatureto reflux for 3 hours
  3. concentrationThe reaction mixture was concentrated in vacuo
  4. customthe residue was purified by silica gel column chromatography
  5. washeluting with CH2Cl2:MeOH 98:2

출처 및 근거

ORD 기록
ord-0a0fbb9b55924b23a84bb909be399f6b
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952008B2

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