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HRID 412668作成日:2026年10月24日

(S)-Benzyl piperidine-2-carboxylate → tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylate

https://huagongshe.com/ja/reaction/412668

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-Benzyl piperidine-2-carboxylateHCID 12436231—
反応物tert-Butyl 2-chloro-1H-benzo[d]imidazole-1-carboxylateHCID 23441223—
生成物tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylateHCID 59063194—

反応手順

The title compound was prepared by a similar method to Preparation 2 from tert-butyl 2-chloro-1H-1,3-benzimidazole-1-carboxylate [see Preparation 46] and benzyl (2S)-2-piperidinecarboxylate [see J.A.C.S. (1 996), 118(7), 1629-1644]. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 90:10 changing to 80:20, by volume, hexane:ethyl acetate, in 5% increments to afford tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylate as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06562964B1
出典データセットuspto-grants-2003_05
ORD IDord-bae9e8ac8db7445da45c38f603f0c930
出典メモuspto-grants-2003_05