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Potassium Carbonate → 2-(3,4-Dimethoxyphenyl)-6-methylimidazo[2,1-b][1,3,4]thiadiazole

HRID 2409528
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HRID 2409528 반응식
Br[C:2]1[S:6][C:5]2=[N:7][C:8]([CH3:10])=[CH:9][N:4]2[N:3]=1.[CH3:11][O:12][C:13]1[CH:14]=[C:15](B(O)O)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20].C([O-])([O-])=O.[K+].[K+]>COCCOC.C(Cl)Cl.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH3:11][O:12][C:13]1[CH:14]=[C:15]([C:2]2[S:6][C:5]3=[N:7][C:8]([CH3:10])=[CH:9][N:4]3[N:3]=2)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]
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참가 물질

7

반응물 3

HCID 11430Potassium CarbonateHCID 27347023,4-Dimethoxyphenylboronic acidHCID 153575782-Bromo-6-methylimidazo[2,1-b][1,3,4]thiadiazole

생성물 1

HCID 667171682-(3,4-Dimethoxyphenyl)-6-methylimidazo[2,1-b][1,3,4]thiadiazole수율 50%

시약·촉매·용매 3

HCID 44119782
Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)
촉매
HCID 6344Dichloromethane용매2회
HCID 80711,2-Dimethoxyethane용매

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온도
130 °C

실험 절차

To a mixture of 2-bromo-6-methyl-imidazo[2,1-b][1,3,4]thiadiazole (0.550 g, 2.522 mmol, 1 eq), 3,4-dimethoxyphenylboronic acid (0.551 g, 3.026 mmol, 1.2 eq) and Pd(dppf)Cl2.DCM (0.209 g. 0.252 mmol, 0.1 eq) in DME (3 mL) was added K2CO3 (1 mL, sat. aq). The mixture was heated in the microwave oven (130° C., 1 h), cooled to RT, diluted with DCM, washed with water, dried (Na2SO4) and concentrated. The residue (yellow solid, 0.720 g) was purified by automated flash chromatography (SiO2, DCM/0-40% MeOH) to give the desired product (yellow solid, 0.347 g, 50%). HPLC-MS (10-95% B in 4 min at 0.5 mL+2 min 100% B, flow 0.8 mL/min, 50° C.): tR=3.77 min, [M+H]+ m/z 276.1.

후처리

  1. temperaturecooled to RT
  2. washwashed with water
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated
  5. customThe residue (yellow solid, 0.720 g) was purified by automated flash chromatography (SiO2, DCM/0-40% MeOH)

출처 및 근거

ORD 기록
ord-c538499f5f7948bd8e4dab435fa1478b
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815918B2

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