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CAS RN: 107819-90-9 | 產品號碼: B4535
N,N'-Bis(tert-butoxycarbonyl)-S-methylisothiourea

純度/分析方法: >98.0%(HPLC)(N)
别名:
- N,N'-Di-Boc-S-methylisothiourea
- Methyl N,N'-Bis(tert-butoxycarbonyl)carbamimidothioate
- N,N'-Bis(tert-butoxycarbonyl)carbamimidothioic Acid Methyl Ester
- Methyl N,N'-Di-Boc-carbamimidothioate
- N,N'-Di-Boc-carbamimidothioic Acid Methyl Ester
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產品規格
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(with Total Nitrogen) | min. 98.0 % |
Melting point | 121.0 to 125.0 °C |
NMR | confirm to structure |
性質
熔點 | 123 °C |
GHS
相關法規
運輸資料
HS編碼* | 2930.90-900 |
Application
A Guanidinylating Reagent
Experimental procedure: To a stirring solution of 1 (272 mg, 0.88 mmol) in anhydrous DMF (10 mL) and N,N'-bis(tert-butoxycarbonyl)-S-methylisothiourea (262 mg, 0.90 mmol) at 0 ℃ is added Et3N (0.37 mL, 2.66 mmol) in one portion, the reaction is stirred for 15 minutes. Then AgNO3 (164 mg, 0.96 mmol) is added, the solution is stirred at 0 ℃ for 3 hours, then room temperature overnight. Filtered the solution through celite, the residue is extracted with water and EtOAc for 3 times. The organic layers are combined and washed with saturated brine, dried over Na2SO4. The crude product is purified by silica gel flash chromatography eluting with 7% EtOAc/hexane to give 2 (455 mg, 86%) as colorless oil.
References
- De Novo Asymmetric Synthesis of (+)-Monanchorin
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