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Sodium hydride → HCID 68181763, 화합물

HRID 1398637
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HRID 1398637 반응식
[I:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][NH:8]2)=[CH:4][CH:3]=1.[H-].[Na+].Cl[C:14]1[N:19]=[CH:18][N:17]=[C:16]([NH2:20])[CH:15]=1>CN(C=O)C>[I:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[C:14]2[N:19]=[CH:18][N:17]=[C:16]([NH2:20])[CH:15]=2)=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 2380124-Amino-6-chloropyrimidineHCID 129912416-iodo-1H-indazole

생성물 1

HCID 68181763HCID 68181763, 화합물수율 35.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
60 °C

실험 절차

To a solution of 6-iodoindazole (500 mg, 2.05 mmol) in DMF (8 mL) was added NaH (60% oil dispersion, 131.12 mg, 3.28 mmol) at 0° C. The mixture was stirred at 0° C. to RT for 10 minutes before addition of 6-chloropyrimidin-4-amine (477.78 mg, 3.69 mmol) and stirring at 60° C. for 17 hr and then transferred to a pressure tube and heated at 70° C. for a further 6 hr. The reaction mixture was cooled and quenched by the addition of water (10 ml) and EtOAc (a few drops) was added. The resultant precipitate was collected by suction filtration and then thoroughly dried under high vacuum to give the title intermediate (248 mg): LC-MS: m/z=+338.20 (M+H)+.

후처리

  1. customtransferred to a pressure tube
  2. temperatureheated at 70° C. for a further 6 hr
  3. temperatureThe reaction mixture was cooled
  4. customquenched by the addition of water (10 ml) and EtOAc (a few drops)
  5. additionwas added
  6. filtrationThe resultant precipitate was collected by suction filtration
  7. customthoroughly dried under high vacuum

출처 및 근거

ORD 기록
ord-8abd5d306d2f495c8d0ad0770f8e0a96
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901313B2

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