Cyanogen Bromide → Methyl 3-aminoimidazo[1,5-a]pyridine-6-carboxylate

HRID 249710노트

반응식

HRID 249710 반응식
FC(F)(F)C(O)=O.[NH2:8][CH2:9][C:10]1[CH:19]=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[CH:12][N:11]=1.C[CH2:21][N:22](C(C)C)C(C)C.N#CBr.C(=O)([O-])O.[Na+]>C1(C)C=CC=CC=1.C(#N)C.O>[NH2:22][C:21]1[N:11]2[CH:12]=[C:13]([C:14]([O:16][CH3:17])=[O:15])[CH:18]=[CH:19][C:10]2=[CH:9][N:8]=1

참가 물질

8

실험 절차

Methyl 6-aminomethylnicotinate trifluoroacetate (390 mg) was dissolved in toluene (35 ml) and treated with Hünig's base (230 μl). Cyanogen bromide (0.35 ml of a 5 M solution in acetonitrile) was then slowly added dropwise. After stirring at RT for 3 h, the solvent was stripped off and the residue was taken up with water and saturated sodium hydrogencarbonate solution and extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and concentrated. The residue was purified by means of preparative HPLC. The product-containing fractions were combined, freed from the acetonitrile and freeze-dried. The residue was then taken up with a little water, treated with saturated sodium hydrogencarbonate solution and extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and concentrated. 110 mg of the desired compound were obtained.

후처리

  1. extractionextracted three times with ethyl acetate
  2. dry with materialThe combined organic phases were dried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe residue was purified by means of preparative HPLC
  6. customfreeze-dried
  7. additiontreated with saturated sodium hydrogencarbonate solution
  8. extractionextracted three times with ethyl acetate
  9. dry with materialThe combined organic phases were dried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6c1e5ec583304f4fb221a93d0576852c
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07863269B2

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