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1,4-Cyclohexadiene → 2-(8-Hydroxy-2-methylimidazo[1,2-a]pyridin-3-yl)acetonitrile

HRID 544469
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HRID 544469 반응식
C([O:8][C:9]1[C:10]2[N:11]([C:15]([CH2:19][C:20]#[N:21])=[C:16]([CH3:18])[N:17]=2)[CH:12]=[CH:13][CH:14]=1)C1C=CC=CC=1.C1CC=CCC=1>[Pd].CN(C)C=O>[C:20]([CH2:19][C:15]1[N:11]2[CH:12]=[CH:13][CH:14]=[C:9]([OH:8])[C:10]2=[N:17][C:16]=1[CH3:18])#[N:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 123431,4-CyclohexadieneHCID 108137Sch 28080

생성물 1

HCID 133382662-(8-Hydroxy-2-methylimidazo[1,2-a]pyridin-3-yl)acetonitrile수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 6228Dimethylformamide용매

실험 절차

8-Benzyloxy-3-cyanomethyl-2-methylimidazo[1,2-a]pyridine (40 g, 0.14 mol), 1,4-cyclohexadiene (50 g, 0.62 mol), dimethylformamide (600 ml) and palladium black (2 g) are stirred together and heated. At 45° C., asudden exotherm occurs and the temperature rises rapidly to 75°-80°. Heating is discontinued and the mixture stirred for1 hr. The catalyst is removed by filtration and the cyclohexadiene removed in vacuo. The dimethylformamide is removed in vacuo (0.1 mm) at 55°to afford 3-cyanomethyl-2-methyl-8-hydroxy imidazo[1,2-a]pyridine (27 g, 0.14 mol).

후처리

  1. temperatureheated
  2. customAt 45° C.
  3. customrises rapidly to 75°-80°
  4. temperatureHeating
  5. customThe catalyst is removed by filtration
  6. customthe cyclohexadiene removed in vacuo
  7. customThe dimethylformamide is removed in vacuo (0.1 mm) at 55°to

출처 및 근거

ORD 기록
ord-3a7ef4a3bdd44203aa43683ad674244f
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04450164

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