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Bromine → HCID 178468688, 화합물

HRID 530835
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HRID 530835 반응식
Cl.[NH:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:8][CH:9]=2)[CH:4]=[N:3]1.[Br:16]Br.C(OCC)(=O)C.CCCCCC>C(O)C>[Br:16][C:4]1[C:5]2[C:10](=[CH:9][CH:8]=[C:7]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:6]=2)[NH:2][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24408Bromine2회HCID 21226206Ethyl acetate hexaneHCID 67984756ethyl 1H-indazole-5-carboxylate hydrochloride

생성물 1

HCID 178468688HCID 178468688, 화합물수율 97.9%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

ethyl 1H-indazole-5-carboxylate hydrochloride (146 g, 0.645 mol) was dissolved in ethanol (4 L, anhydrous). Bromine (113.3 g, 0.709 mol) in 200 ethanol was added at room temperature. The reaction mixture was allowed to stir for 17 hours at room temperature. TLC (30% ethyl acetate/hexane) indicated that starting material was left. Bromine (40 g in 100 mL of ethanol) was added at room temperature. After 1 hour, TLC indicated no starting material was left. Ethanol was evaporated (2 L removed) and the mixture was poured into ice-water (8 L). The purple solid was stirred and 750 mL of saturated Na2S2O3 and NaOH solution was added to adjust the pH to 10-11. Total volume was 10 L. The mixture was stirred for 30 minutes and the solid were filtered and washed with 1.5 L of water and dried in a vacuum oven to obtain 170 gram of product as yellow solid.

후처리

  1. waitwas left
  2. waitAfter 1 hour
  3. waitwas left
  4. customEthanol was evaporated
  5. custom(2 L removed)
  6. additionthe mixture was poured into ice-water (8 L)
  7. stirringThe purple solid was stirred
  8. addition750 mL of saturated Na2S2O3 and NaOH solution was added
  9. stirringThe mixture was stirred for 30 minutes
  10. filtrationthe solid were filtered
  11. washwashed with 1.5 L of water
  12. customdried in a vacuum oven

출처 및 근거

ORD 기록
ord-36eb59c71bf74da797faef65fe8d24d8
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09351965B2

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