참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Diazomethane | HCID 9550 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 반응물 | 2-(4-chloro-N-(pent-1-yn-3-yl)phenylsulfonamido)-butanoic acid | HCID 59342373 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 4-chloro-N-(1-diazo-2-oxopentan-3-yl)-N-(pent-1-yn-3-yl)benzenesulfonamide | HCID 72259587 | — |
반응 단계
To a solution of the compound 60 (498 mg, 1.45 mmol) in 7.5 mL of Et2O were added sequentially 0.24 mL of triethylamine (1.2 eq), 0.23 mL of isobutyl chloroformate (1.2 eq) at −30° C. After being stirred at −30° C. for 15 min, diazomethane (prepared by mixing MNNG and KOH in diethyl ether) (excess) was added to the above mixture at 0° C. and stirred there for 5 hours. Glacial HOAc (1.5 mL) was added to destroy the excess diazomethane and the solution was extracted with EtOAc. The organic phase was washed with sat NaHCO3, water, brine and dried (MgSO4). LCMS 368.1 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07732609B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-c6a04bb7504c4ce18d8cc8e65ca5dd39 |
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| 출처 메모 | uspto-grants-2010_06 |
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