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Methane → 10-isobutyramido-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one

HRID 1290767
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HRID 1290767 반응식
Cl.[NH2:2][CH:3]1[C:15]2[N:14]3[CH:16]=[CH:17][N:18]=[C:13]3[C:12](=[O:19])[NH:11][C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]1=2.[C:20](Cl)(=[O:24])[CH:21]([CH3:23])[CH3:22].C(N(CC)CC)C.C>CN(C)C=O.CO>[C:20]([NH:2][CH:3]1[C:15]2[N:14]3[CH:16]=[CH:17][N:18]=[C:13]3[C:12](=[O:19])[NH:11][C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]1=2)(=[O:24])[CH:21]([CH3:23])[CH3:22]
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참가 물질

7

반응물 4

HCID 297MethaneHCID 8471TriethylamineHCID 62325Isobutyryl chloride2회HCID 1897547210-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one hydrochloride

생성물 1

HCID 1891816710-isobutyramido-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one수율 33.9%

시약·촉매·용매 2

HCID 887
Methanol
용매
HCID 6228Dimethylformamide용매2회

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온도
-10 °C

실험 절차

To a suspension of 1 g of 10-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one hydrochloride in 50 ml of anhydrous dimethylformamide, maintained under an argon atmosphere at a temperature in the region of -10° C., are successively added 0.9 g of isobutyryl chloride and a solution of 0.4 g of triethylamine in 5 ml of anhydrous dimethylformamide. The mixture is stirred for 1 hour at the same temperature and 0.4 g of isobutyryl chloride is added. The mixture is stirred for 30 minutes at the same temperature and for 1 hour while allowing the temperature to return gradually to 20° C. The insoluble material formed is removed by filtration and the filtrate is concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 70° C. The product obtained (1.63 g) is dissolved in 30 ml of methanol and, after addition of decolorizing charcoal, the solution is filtered, diluted with 40 ml of distilled water and stored for 45 minutes at a temperature in the region of 20° C. The insoluble material formed is separated out by filtration, washed with 5 ml of distilled water and with 5 ml of acetone and then dried under reduced pressure (1 mmHg; 0.13 kPa) at 100° C. 0.38 g of 10-isobutyramido-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one is thus obtained, decomposing without melting above 260° C. [N.M.R. spectrum: [300 MHz; (CD3)2SO d6 ; δ in ppm]: 1.09 and 1.12 [2d, J=7.5 Hz, 6H: --CH(CH3)2 ]; 2.48 [mt, 1H: --CH(CH3)2 ]; 6.15 (d, J=8.5 Hz, 1H: --CH-- 10); 7.35 and 7.45 (2t broad, J=8.5 Hz, 1H each: --H7 and --H8); 7.47 and 7.85 (2d broad, J=8 Hz, 1H each: --H6 and --H9); 7.52 and 7.58 (2s, 1H each: --H of the imidazole); 8.46 (d, J=8.5 Hz, 1H: --NHCO-- at 10); 12.48 (broad s, 1H: --CONH-- of the ring)].

후처리

  1. additionis added
  2. customto return gradually to 20° C
  3. customThe insoluble material formed
  4. customis removed by filtration
  5. concentrationthe filtrate is concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 70° C
  6. customThe product obtained (1.63 g)
  7. filtrationthe solution is filtered
  8. additiondiluted with 40 ml of distilled water
  9. waitstored for 45 minutes at a temperature in the region of 20° C
  10. customThe insoluble material formed
  11. customis separated out by filtration
  12. washwashed with 5 ml of distilled water and with 5 ml of acetone
  13. customdried under reduced pressure (1 mmHg; 0.13 kPa) at 100° C

출처 및 근거

ORD 기록
ord-96683e19caa9458bbc509fd3476c4292
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753657

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