참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | 2-Aminobenzimidazole | HCID 13624 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-(Methylsulfonyl)-1H-Benzimidazol-2-Amine | HCID 22997045 | 28.7% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06613743B2 |
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| 출처 데이터셋 | uspto-grants-2003_09 |
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| ORD ID | ord-e511ac310c7442fcb3fc872f72a287c5 |
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| 출처 메모 | uspto-grants-2003_09 |
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