Trichloroisocyanuric Acid → 4-[(2-isopropoxyethyl)amino]-1H-imidazole-5-carboxamide

HRID 548783

반응식

HRID 548783 반응식
ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O.[CH:13]([O:16][CH2:17][CH2:18]O)([CH3:15])[CH3:14].Cl.[NH2:21][C:22]1[N:23]=[CH:24][NH:25][C:26]=1[C:27]([NH2:29])=[O:28]>C(Cl)Cl.CO.CC1(C)N([O])C(C)(C)CCC1>[CH:13]([O:16][CH2:17][CH2:18][NH:21][C:22]1[N:23]=[CH:24][NH:25][C:26]=1[C:27]([NH2:29])=[O:28])([CH3:14])[CH3:15]

참가 물질

7

반응 조건

온도
0 °C

실험 절차

Trichlorocyanuric acid (1.23 g, 5.29 mmol) was added to a solution of 2-isopropoxyethanol (0.50 g, 4.80 mmol) in CH2Cl2 (3 mL). The reaction mixture was cooled to 0° C. and TEMPO (0.015 g, 0.09 mmol) was carefully added in small portions. The mixture was stirred at r.t. for 20 minutes and then filtrated through Celite and washed with CH2Cl2. The filtrate was kept cold, 0° C., during the filtration. The obtained aldehyde solution was added to a stirred mixture of 4-amino-1H-imidazole-5-carboxamide hydrochloride (0.78 g, 4.80 mmol), which was obtained from Example 3(b), at 0° C. in MeOH (5 mL). The mixture was stirred for 20 minutes, then NaCNBH4 (0.30 g, 4.80 mmol) was added. After stirring at r.t for 5 h the mixture was concentrated and purified by flash chromatography (CH2Cl2/methanol gradient; 0 to 5% methanol), to yield the title compound (0.39 g, 38%) as an oil.

후처리

  1. filtrationfiltrated through Celite
  2. washwashed with CH2Cl2
  3. filtrationThe filtrate was kept cold, 0° C., during the filtration
  4. stirringThe mixture was stirred for 20 minutes
  5. additionNaCNBH4 (0.30 g, 4.80 mmol) was added
  6. stirringAfter stirring at r.t for 5 h the mixture
  7. concentrationwas concentrated
  8. custompurified by flash chromatography (CH2Cl2/methanol gradient; 0 to 5% methanol)

출처 및 근거

ORD 기록
ord-6673139033054c94a3ee28934054b163
출처 데이터셋
uspto-grants-2011_05
특허 번호
US07943625B2

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