Dimethylformamide → 1-(Methylsulfonyl)-1H-Benzimidazol-2-Amine

HRID 1166461

반응식

HRID 1166461 반응식
[NH2:1][C:2]1[NH:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.CN(C=O)C.[CH3:16][S:17](Cl)(=[O:19])=[O:18]>C(Cl)Cl>[CH3:16][S:17]([N:3]1[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=[C:2]1[NH2:1])(=[O:19])=[O:18]

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 136242-AminobenzimidazoleHCID 31297Methanesulfonyl chloride

생성물 1

HCID 229970451-(Methylsulfonyl)-1H-Benzimidazol-2-Amine수율 28.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

2-amino-benzimidazole (1.0 g, 7.5 mmol) was dissolved in 15 mL of anhydrous CH2Cl2 and 3 mL anhydrous DMF and cooled to ˜0° C. Trethylamine(1.6 mL, 1.5 eq.) was added followed by an addition of methanesulfonylchloride (580 μL, 7.5 mmol) over 1 minute. After 1 minute at ˜0° C., the reaction was warmed to RT. After 1 hour the reaction was quenched with water, and partitioned between a saturated sodium bicarbonate solution and CH2Cl2. The aqueous layer was extracted with CH2Cl2 and the combined organic layers were washed with water (2 times), brine then dried over NaSO4, filtered and the solvent was removed in vacuo to give 455 mg of N-methanesulfonyl-2-aminobenzimidazole. HPLC shows the material to be 91% pure, (ret. time=3.70). LCMS: obs. [email protected] amu. The material was carried on without purification.

후처리

  1. additionTrethylamine(1.6 mL, 1.5 eq.) was added
  2. customAfter 1 hour the reaction was quenched with water
  3. custompartitioned between a saturated sodium bicarbonate solution and CH2Cl2
  4. extractionThe aqueous layer was extracted with CH2Cl2
  5. washthe combined organic layers were washed with water (2 times), brine
  6. dry with materialthen dried over NaSO4
  7. filtrationfiltered
  8. customthe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-e511ac310c7442fcb3fc872f72a287c5
출처 데이터셋
uspto-grants-2003_09
특허 번호
US06613743B2

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