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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Phosphorus tribromide → 1372891-51-4

HRID 1625066
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HRID 1625066 반응식
[F:1][C:2]1[C:3]([CH2:9]O)=[N:4][CH:5]=[CH:6][C:7]=1[CH3:8].P(Br)(Br)[Br:12]>C1COCC1>[Br:12][CH2:9][C:3]1[C:2]([F:1])=[C:7]([CH3:8])[CH:6]=[CH:5][N:4]=1
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참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 68277844HCID 68277844, 화합물

생성물 1

HCID 866916061372891-51-4수율 104.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Intermediate 6 ((3-fluoro-4-methyl-2-pyridinyl)methanol, 246 mg, 1.743 mmol) was dissolved in 10 mL of anhydrous THF. Phosphorous tribromide (ALDRICH, 519 mg, 1.917 mmol) was added. Reaction mixture was stirred at room temperature overnight. Solvent was evaporated and residue was partitioned between Et2O and NaHCO3 (aqueous saturated solution). Organic layer was dried over MgSO4 (anh), filtered and concentrated to give the title compound (372 mg, quantitative yield). 1H NMR (300 MHz, DMSO-d6) δ ppm: 8.23-8.24 (m, 1H), 7.34-7.37 (m, 1H), 4.66 (s, 2H), 2.28 (s, 3H). [ES+MS] m/z 204 (M).

후처리

  1. customReaction mixture
  2. customSolvent was evaporated
  3. customresidue was partitioned between Et2O and NaHCO3 (aqueous saturated solution)
  4. dry with materialOrganic layer was dried over MgSO4 (anh)
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-00520d7642d740b1abd77cf5b68907aa
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08779153B2

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