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(S)-Benzyl piperidine-2-carboxylate → tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (S)-Benzyl piperidine-2-carboxylate | HCID 12436231 | — |
| 反応物 | tert-Butyl 2-chloro-1H-benzo[d]imidazole-1-carboxylate | HCID 23441223 | — |
| 生成物 | tert-butyl 2-[(2S)-2-[(benzyloxy)carbonyl]-1-piperidinyl]-1H-1,3-benzimidazole-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06562964B1 |
| 出典データセット | uspto-grants-2003_05 |
| ORD ID | ord-bae9e8ac8db7445da45c38f603f0c930 |
| 出典メモ | uspto-grants-2003_05 |