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1,1'-Carbonyldiimidazole → HCID 86694158, 화합물

HRID 707290
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HRID 707290 반응식
[Br:1][C:2]1[N:7]=[C:6]([NH:8][CH:9]2[CH2:11][CH2:10]2)[C:5]([NH2:12])=[N:4][CH:3]=1.[C:13](N1C=CN=C1)(N1C=CN=C1)=[O:14]>C1COCC1>[Br:1][C:2]1[N:7]=[C:6]2[N:8]([CH:9]3[CH2:10][CH2:11]3)[C:13](=[O:14])[NH:12][C:5]2=[N:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 682631,1'-Carbonyldiimidazole2회HCID 86694157HCID 86694157, 화합물

생성물 1

HCID 86694158HCID 86694158, 화합물수율 57%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
66 °C

실험 절차

To a heated (50° C.) solution of 6-bromo-N2-cyclopropylpyrazine-2,3-diamine (0.740 g, 3.23 mmol) in THF (20 mL) was added 1,1′-carbonyldiimidazole (1.00 g, 6.17 mmol) in one portion. The reaction was then heated at 66° C. for 3 h. Additional 1,1′-carbonyldiimidazole (1.00 g, 6.17 mmol) was added and the reaction was heated at 50° C. overnight. The reaction was cooled to room temperature and carefully quenched with water (slight exotherm) until gas evolution ceased. The solution was diluted with EtOAc and the layer were separated. The organic layer was washed with water (1×) and brine (1×). The solution was evaporated onto silica gel and purified by flash chromatography (ISCO(40 gram)) eluting with EtOAc:hexanes (0:1→2:3) to give 467 mg (57%) of a yellow crystalline solid. ESI MS 256.9 [M+1].

후처리

  1. temperaturethe reaction was heated at 50° C. overnight
  2. temperatureThe reaction was cooled to room temperature
  3. customcarefully quenched with water (slight exotherm) until gas evolution
  4. additionThe solution was diluted with EtOAc
  5. customthe layer were separated
  6. washThe organic layer was washed with water (1×) and brine (1×)
  7. customThe solution was evaporated onto silica gel
  8. custompurified by flash chromatography (ISCO(40 gram))
  9. washeluting with EtOAc:hexanes (0:1→2:3)

출처 및 근거

ORD 기록
ord-0a13f5e878134c1787c7117981ee1b8c
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174992B2

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