Hydrochloric Acid → 2-(Thieno[2,3-d]pyridazin-3-yl)furo[2,3-c]pyridin-7-amine

HRID 389552노트

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HRID 389552 반응식
C(OC([N:8](C(OC(C)(C)C)=O)[C:9]1[N:10]=[CH:11][CH:12]=[C:13]2[CH:17]=[C:16](B(O)O)[O:15][C:14]=12)=O)(C)(C)C.Br[C:29]1[C:37]2[C:32](=[CH:33][N:34]=[N:35][CH:36]=2)[S:31][CH:30]=1.C(=O)([O-])[O-].[K+].[K+].Cl.C(=O)(O)[O-].[Na+]>O1CCOCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O>[S:31]1[C:32]2=[CH:33][N:34]=[N:35][CH:36]=[C:37]2[C:29]([C:16]2[O:15][C:14]3=[C:9]([NH2:8])[N:10]=[CH:11][CH:12]=[C:13]3[CH:17]=2)=[CH:30]1

참가 물질

9

반응물 5

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 516892Sodium BicarbonateHCID 228926363-Bromothieno[2,3-d]pyridazineHCID 66761297{7-[Bis(tert-butoxycarbonyl)amino]furo[2,3-c]pyridin-2-yl}boronic acid

생성물 1

HCID 667606692-(Thieno[2,3-d]pyridazin-3-yl)furo[2,3-c]pyridin-7-amine수율 31.9%

시약·촉매·용매 3

HCID 178418397HCID 178418397, 화합물촉매HCID 962Water용매HCID 312751,4-Dioxane용매2회

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온도
70 °C

실험 절차

A suspension of {7-[bis(tert-butoxycarbonyl)amino]furo[2,3-c]pyridin-2-yl}boronic acid (200.0 mg, 0.5288 mmol), 3-bromothieno[2,3-d]pyridazine (77.1 mg, 0.358 mmol), Pd(PPh3)4 (21.8 mg, 0.0189 mmol), and potassium carbonate (150.5 mg, 1.089 mmol) in a 4:1 mixture of 1,4-dioxane to water (3.5 mL) was heated conventionally to 70° C. for 2.5 h. To the stirring reaction at 70° C., 4.0 M hydrochloric acid in 1,4-dioxane (2.0 mL) was added and was stirred for 1 h. The reaction mixture was cooled to ambient temperature, poured into saturated aqueous sodium bicarbonate, and extracted with dichloromethane. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. Purification by ISCO chromatography (3 to 15% methanol:dichloromethane) afforded 30.6 mg (31%) of the title compound as a yellow solid. 1H NMR (400 MHz, DMF-d7): δ 10.43 (d, J=1.52 Hz, 1H), 10.10 (d, J=1.52 Hz, 1H), 8.92 (s, 1H), 7.83 (d, J=5.31 Hz, 1H), 7.67 (s, 1H), 6.95 (d, J=5.31 Hz, 1H), 6.66 (br s, 2H); MS (ESI): 269.13 [M+H]+; HPLC tR=2.16 min.

후처리

  1. customTo the stirring reaction at 70° C.
  2. temperatureThe reaction mixture was cooled to ambient temperature
  3. extractionextracted with dichloromethane
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification by ISCO chromatography (3 to 15% methanol:dichloromethane)

출처 및 근거

ORD 기록
ord-cd39c6b953274cb6a9a4e637b45cc908
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08378104B2

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