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Chlorotrimethylsilane → 3-(4-Boronophenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acid

HRID 1424315
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HRID 1424315 반응식
[NH2:1][CH:2]([CH2:6][C:7]1[CH:12]=[CH:11][C:10]([B:13]([OH:15])[OH:14])=[CH:9][CH:8]=1)[C:3]([OH:5])=[O:4].CCN(C(C)C)C(C)C.C[Si](Cl)(C)C.[CH3:30][C:31]1[CH:39]=[C:38]([CH3:40])[CH:37]=[C:36]([CH3:41])[C:32]=1[C:33](Cl)=[O:34]>C(Cl)Cl>[B:13]([C:10]1[CH:11]=[CH:12][C:7]([CH2:6][CH:2]([NH:1][C:33](=[O:34])[C:32]2[C:36]([CH3:41])=[CH:37][C:38]([CH3:40])=[CH:39][C:31]=2[CH3:30])[C:3]([OH:5])=[O:4])=[CH:8][CH:9]=1)([OH:15])[OH:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6397ChlorotrimethylsilaneHCID 53503p-BoronophenylalanineHCID 81531DiisopropylethylamineHCID 970382,4,6-Trimethylbenzoyl chloride

생성물 1

HCID 576609483-(4-Boronophenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acid

시약·촉매·용매 1

HCID 6344Dichloromethane
용매
3회

실험 절차

1.5 g (7.18 mmol) of 2-amino-3-(4-boronophenyl)propionic acid were suspended in 50 ml DCM and 7.4 ml (43.1 mmol) DIPEA and refluxed for 20 min together with 4.5 ml (35 mmol) TMSCl. The solution was cooled in an ice bath and a solution of 1.44 g (7.9 mmol) 2,4,6-trimethylbenzoyl chloride in 5 ml DCM were added dropwise. The reaction mixture was stirred 2 h at room temperature, diluted with 100 ml DCM and washed with 2 N aqueous HCl. During this washing some product precipitated which was collected. The organic phase was extracted with 2 N NaOH twice. Upon acidifying of the combined basic phases the product precipitated, which was collected and dried together with the first precipitate. The crude product was used without further purification.

후처리

  1. temperatureThe solution was cooled in an ice bath
  2. washwashed with 2 N aqueous HCl
  3. customDuring this washing some product precipitated which
  4. customwas collected
  5. extractionThe organic phase was extracted with 2 N NaOH twice
  6. customprecipitated
  7. customwhich was collected
  8. customdried together with the first precipitate
  9. customThe crude product was used without further purification

출처 및 근거

ORD 기록
ord-0c7bef94f99d4f2da8782cb9b47e5567
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927534B2

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