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Acetic Acid → 2-Hydroxymethyl-1-methylimidazo[4,5-c]pyridine

HRID 1601844
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HRID 1601844 반응식
[Si]([O:8][CH2:9][C:10]1[N:11]([CH3:19])[C:12]2[CH:17]=[CH:16][N:15]=[CH:14][C:13]=2[N:18]=1)(C(C)(C)C)(C)C.O1CCCC1.C(O)(=O)C>O>[OH:8][CH2:9][C:10]1[N:11]([CH3:19])[C:12]2[CH:17]=[CH:16][N:15]=[CH:14][C:13]=2[N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 8028TetrahydrofuranHCID 232983402-t-Butyldimethylsilyloxymethyl-1-methylimidazo[4,5-c]pyridine

생성물 1

HCID 232983682-Hydroxymethyl-1-methylimidazo[4,5-c]pyridine수율 111.6%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of 3.00 g of 2-t-butyldimethylsilyloxymethyl-1-methyl-1H-imidazo[4,5-c]pyridine (prepared as described in Preparation 72) in 60 ml of a 1:1:1 by volume mixture of tetrahydrofuran, acetic acid and water was stirred at room temperature for 1 hour and then at 60° C. for 5 hours. At the end of this time, the reaction mixture was freed from the solvent by distillation. The resulting residue was mixed with an aqueous solution of sodium hydrogencarbonate and then concentrated by evaporation under reduced pressure. The concentrate was purified by column chromatography through silica gel, using a 10:1 by volume mixture of ethyl acetate and methanol as the eluent, to give 1.97 g of the title compound, melting at 285-290° C.

후처리

  1. waitat 60° C. for 5 hours
  2. distillationAt the end of this time, the reaction mixture was freed from the solvent by distillation
  3. additionThe resulting residue was mixed with an aqueous solution of sodium hydrogencarbonate
  4. concentrationconcentrated by evaporation under reduced pressure
  5. customThe concentrate was purified by column chromatography through silica gel
  6. additionby volume mixture of ethyl acetate and methanol as the eluent

출처 및 근거

ORD 기록
ord-f84ebd1157f84eaab917ba7b27795812
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05977365

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