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Phosphorus pentabromide → 1-Bromo-4-oxo-3,4-dihydro-phthalazine-6-carboxylic acid

HRID 1783720
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HRID 1783720 반응식
O=[C:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([OH:14])=[O:13])=[CH:9][CH:10]=2)[C:5](=[O:15])[NH:4][NH:3]1.P(Br)(Br)(Br)(Br)[Br:17]>ClCCCl.CC(O)=O>[Br:17][C:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([OH:14])=[O:13])=[CH:9][CH:10]=2)[C:5](=[O:15])[NH:4][N:3]=1
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참가 물질

5

반응물 2

HCID 62678Phosphorus pentabromideHCID 3090561,4-Dioxo-1,2,3,4-tetrahydrophthalazine-6-carboxylic acid

생성물 1

HCID 211065111-Bromo-4-oxo-3,4-dihydro-phthalazine-6-carboxylic acid수율 73%

시약·촉매·용매 2

HCID 111,2-Dichloroethane용매HCID 176Acetic Acid용매

실험 절차

1,4-Dioxo-1,2,3,4-tetrahydro-phthalazine-6-carboxylic acid (91.0 g, 0.44 mol) was suspended in DCE (1.0 L) and phosphorus pentabromide (761.0 g, 1.77 mol) was added in three portions and the reaction heated to reflux for 24 hours. The reaction was cooled to RT and poured onto ice (2.5 kg) and the resulting precipitate filtered and washed with water to give the crude product (130.0 g). This crude material was suspended in HOAc (1.6 L) and heated to 125° C. for 2 h. The reaction was cooled to RT and poured onto ice (1.5 kg) and the resulting precipitate filtered. The solid was washed with water and dried to give the title compound (85 g, 73% yield) as a yellow solid. Tr=0.94 min, m/z (ES+) (M+H)+ 310 & 312

후처리

  1. temperaturethe reaction heated
  2. temperatureto reflux for 24 hours
  3. additionpoured onto ice (2.5 kg)
  4. filtrationthe resulting precipitate filtered
  5. washwashed with water
  6. customto give the crude product (130.0 g)
  7. temperatureheated to 125° C. for 2 h
  8. temperatureThe reaction was cooled to RT
  9. additionpoured onto ice (1.5 kg)
  10. filtrationthe resulting precipitate filtered
  11. washThe solid was washed with water
  12. customdried

출처 및 근거

ORD 기록
ord-838951553ef546c1973ea38e16219174
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07501410B2

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