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Hydrochloric Acid → HCID 20042545, 화합물

HRID 1762219
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HRID 1762219 반응식
[OH:1][CH2:2][C:3]1[CH:23]=[CH:22][CH:21]=[C:20]([CH2:24][OH:25])[C:4]=1[CH2:5][O:6][C:7]1[C:8]2[N:9]([C:13]([CH2:17][C:18]#[CH:19])=[C:14]([CH3:16])[N:15]=2)[CH:10]=[CH:11][CH:12]=1.[ClH:26]>CO>[ClH:26].[OH:25][CH2:24][C:20]1[CH:21]=[CH:22][CH:23]=[C:3]([CH2:2][OH:1])[C:4]=1[CH2:5][O:6][C:7]1[C:8]2[N:9]([C:13]([CH2:17][C:18]#[CH:19])=[C:14]([CH3:16])[N:15]=2)[CH:10]=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 14368371HCID 14368371, 화합물

생성물 1

HCID 20042545HCID 20042545, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a suspension of 8-[2,6-bis(hydroxymethyl)benzyloxy]-2-methyl-3-(2-propynyl)imidazo[1,2-a]pyridine (4.9 g) in methanol (80 ml) was added 1 N hydrochloric acid (15 ml) at room temperature. The obtained clear solution was concentrated under reduced pressure and the residue was recrystallized from a mixture of acetone (100 ml) and water (8 ml) to give 8-[2,6-bis(hydroxymethyl)benzyloxy]-2-methyl-3-(2-propynyl)imidazo[1,2-a]pyridine hydrochloride (4.44g)

후처리

  1. concentration
The obtained clear solution was concentrated under reduced pressure
  • customthe residue was recrystallized from a mixture of acetone (100 ml) and water (8 ml)
  • 출처 및 근거

    ORD 기록
    ord-fffe213b2c31483d8ab90bc9aa2ca561
    출처 데이터셋
    uspto-grants-1989_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04831041

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