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p-Toluenesulfonic acid monohydrate → 6-Bromo-5-(2,4-difluorophenoxy)-1H-benzimidazole

HRID 629307
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HRID 629307 반응식
[Br:1][C:2]1[CH:3]=[C:4]([NH2:18])[C:5]([NH2:17])=[CH:6][C:7]=1[O:8][C:9]1[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=1[F:16].[CH:19]([O-])([O-])OCC.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>O1CCCC1>[Br:1][C:2]1[C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=2[F:16])=[CH:6][C:5]2[N:17]=[CH:19][NH:18][C:4]=2[CH:3]=1
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참가 물질

5

반응물 3

HCID 521998p-Toluenesulfonic acid monohydrateHCID 53630039EthylorthoformateHCID 1180936764-Bromo-5-(2,4-difluorophenoxy)benzene-1,2-diamine

생성물 1

HCID 1180936296-Bromo-5-(2,4-difluorophenoxy)-1H-benzimidazole수율 75.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
50 °C

실험 절차

A solution of 4-bromo-5-(2,4-difluorophenoxy)benzene-1,2-diamine (0.090 g, 0.28 mmol) in tetrahydrofuran (1.1 mL) was treated with ethyl orthoformate (0.142 mL, 0.857 mmol) followed by p-toluenesulfonic acid monohydrate (0.005 g, 0.03 mmol) and stirred at 50° C. for 1 h. The reaction mixture was concentrated and diluted with ethyl acetate and saturated sodium bicarbonate. The organic layer was separated and washed with brine, dried with magnesium sulfate, filtered, and concentrated to give a crude oil. Purification by flash column chromatography (100% hexanes to 100% EtOAc) gave the desired product (69 mg, 74%). LCMS calculated for C13H8BrF2N2O (M+H)+: m/z=325.0, 327.0. found: 325.0, 327.0.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with ethyl acetate and saturated sodium bicarbonate
  3. customThe organic layer was separated
  4. washwashed with brine
  5. dry with materialdried with magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto give a crude oil
  9. customPurification by flash column chromatography (100% hexanes to 100% EtOAc)

출처 및 근거

ORD 기록
ord-6d300c234c854629bd1c6dbd695af6fb
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315501B2

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