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HRID 1012912作成日:2026年10月26日

Water → [4-(Benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1012912

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物BenzothiazoleHCID 7222—
反応物ButyllithiumHCID 178418339—
反応物HCID 178502731HCID 178502731—
溶媒TetrahydrofuranHCID 8028—
生成物[4-(Benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl esterHCID 6731716682.1%

反応手順

To a solution of benzothiazole (675 mg, 0.55 ml, 5 mmol) in THF (20 ml) at −78° C. was added dropwise n-BuLi (2.5M in Hex, 2 ml) such that the temperature did not exceed −70° C. The brown solution was stirred at this temperature for 15 min before dropwise addition of a solution of [trans-4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester (716 mg, 2.5 mmol, prepared according to WO 03/053933) in THF (2 ml). The temperature was kept below −70° C. The brown solution was then gradually allowed to reach RT (over 3 h). Mixture was poured into water and extracted with EtOAc. The combined organic extracts were washed with brine and dried over MgSO4 and concentrated under reduced pressure. The residue was purified by chromatography over SiO2 (Hex/EtOAc 4:1 then DCM). The relevant fractions were pooled, evaporated under reduced pressure, digested with Hex and filtered to give 740 mg (82%) of [4-(benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981886B2
出典データセットuspto-grants-2011_07
ORD IDord-35a01e6be0c24725a8d37793c2468181
出典メモuspto-grants-2011_07