Hydrochloric Acid → HCID 71280499, 화합물

HRID 1045439노트

반응식

HRID 1045439 반응식
FC(F)O[C:4]1[CH:9]=[CH:8][N:7]2[C:10]([C:13]([O:15]CC)=[O:14])=[CH:11][N:12]=[C:6]2[CH:5]=1.[Li+].[OH-:20].Cl>C1COCC1.CO>[O:20]=[C:4]([CH3:9])[CH2:5][CH2:6][C:9]1[CH:4]=[CH:5][C:6]2[N:7]([C:10]([C:13]([OH:15])=[O:14])=[CH:11][N:12]=2)[CH:8]=1

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 71280851HCID 71280851, 화합물

생성물 1

HCID 71280499HCID 71280499, 화합물

시약·촉매·용매 1

HCID 21899815MeOH tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

A stirring mixture of ethyl 7-(difluoromethoxy)imidazo[1,2-a]pyridine-3-carboxylate (79) (150 mg, 0.585 mmol) and 2N LiOH (1 mL) in THF:MeOH (4:1, 5 mL) was heated at 60° C. for 45 minutes. The reaction was cooled to room temperature and the pH was adjusted between 4-5 with 1N HCl. The solvent was partially reduced and the crude product was purified by reverse phase preparative HPLC to yield 6-(3-oxobutyl)imidazo[1,2-a]pyridine-3-carboxylic acid (80). MS m/z 229.03 (M+1)+.

후처리

  1. temperatureThe reaction was cooled to room temperature
  2. customthe crude product was purified by reverse phase preparative HPLC

출처 및 근거

ORD 기록
ord-cf4f1e184f714fc19dac504c89da8d2e
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08569283B2

반응 노트

불러오는 중…