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Sodium Bicarbonate → 2-bromo-3-chloro-5H-pyrrolo[2,3-b]pyrazine

HRID 523024
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HRID 523024 반응식
[Br:1][C:2]1[N:3]=[C:4]([C:10]#[C:11][Si](C)(C)C)[C:5]([NH2:9])=[N:6][C:7]=1[Cl:8].CC([O-])(C)C.[K+].C([O-])(O)=O.[Na+]>C1COCC1.O>[Br:1][C:2]1[N:3]=[C:4]2[CH:10]=[CH:11][NH:9][C:5]2=[N:6][C:7]=1[Cl:8]
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참가 물질

6

반응물 3

HCID 516892Sodium BicarbonateHCID 23665647Potassium tert-butoxideHCID 900409205-Bromo-6-chloro-3-trimethylsilanylethynyl-pyrazin-2-ylamine

생성물 1

HCID 900413612-bromo-3-chloro-5H-pyrrolo[2,3-b]pyrazine수율 107.2%

시약·촉매·용매 2

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매
2회

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온도
0 °C

실험 절차

To a stirred solution of 5-bromo-6-chloro-3-trimethylsilanylethynyl-pyrazin-2-ylamine (2.0 g, 6.58 mmol) in THF (28 mL) was added a 1 M solution of KOtBu in THF (7.24 mL, 7.24 mmol) slowly at 0° C. under a nitrogen atmosphere. The reaction mixture was stirred at 0° C. for 10 min and then warmed to room temperature. After 2 h, the mixture was concentrated in vacuo and the residue obtained was suspended in water (7.5 mL) and saturated aqueous NaHCO3 (7.5 mL) and stirred overnight at room temperature The solid was filtered, washed with water and hexanes then dried in an oven at 80° C. to give 2-bromo-3-chloro-5H-pyrrolo[2,3-b]pyrazine (1.64 g) as brown solid. LC-MS: 232 (M−H). This was used directly without further purification.

후처리

  1. temperaturewarmed to room temperature
  2. waitAfter 2 h
  3. concentrationthe mixture was concentrated in vacuo
  4. customthe residue obtained
  5. filtrationwas filtered
  6. washwashed with water and hexanes
  7. customthen dried in an oven at 80° C.

출처 및 근거

ORD 기록
ord-e8f33d4dadd64556a80205e3d01effdf
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09334278B2

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