Sodium Hydroxide → S-[2-(1-benzyloxycarbonyl-4-piperidyl)ethyl]-L-cysteine

HRID 1638988

反応式

HRID 1638988 の反応式
O.Cl.[NH2:3][C@H:4]([C:7]([OH:9])=[O:8])[CH2:5][SH:6].[OH-].[Na+].[CH2:12]([O:19][C:20]([N:22]1[CH2:27][CH2:26][CH:25]([CH2:28][CH2:29]I)[CH2:24][CH2:23]1)=[O:21])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(O)C>[CH2:12]([O:19][C:20]([N:22]1[CH2:27][CH2:26][CH:25]([CH2:28][CH2:29][S:6][CH2:5][C@@H:4]([C:7]([OH:9])=[O:8])[NH2:3])[CH2:24][CH2:23]1)=[O:21])[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

参加物

5

反応物 3

HCID 14798Sodium HydroxideHCID 23462L-Cysteine hydrochloride monohydrateHCID 14600697Benzyl 4-(2-iodoethyl)piperidine-1-carboxylate

生成物 1

HCID 14600699S-[2-(1-benzyloxycarbonyl-4-piperidyl)ethyl]-L-cysteine収率 68.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

In a nitrogen gas flow, 562 mg of L-cysteine hydrochloride monohydrate is dissolved in an aqueous solution of 2N sodium hydroxide. To the resulting solution, 5 ml of a tetrohydrofuran solution containing 1.2 g of 2-(1-benzyloxycarbonyl-4-piperidyl)ethyl iodide is added, and stirred for 1.5 hours at room temperature. Then, 3 ml of ethanol is further added, and stirred for 2 hours. The reaction solvent is distilled off under reduced pressure. To the residue, water and ether are added, and the mixture is shaken. The water layer is separated and adjusted to pH 5 with 2N aqueous hydrochloric acid to precipitate crystals. The crystals are recrystallized from methanol to give 0.8 g of S-[2-(1-benzyloxycarbonyl-4-piperidyl)ethyl]-L-cysteine having a melting point of 185° to 188° C.

後処理

  1. additionis added
  2. stirringstirred for 2 hours
  3. distillationThe reaction solvent is distilled off under reduced pressure
  4. additionTo the residue, water and ether are added
  5. stirringthe mixture is shaken
  6. customThe water layer is separated
  7. customto precipitate crystals
  8. customThe crystals are recrystallized from methanol

出典と根拠

ORDレコード
ord-a4b00b691d984251b8563c73cf233717
出典データセット
uspto-grants-1989_11
特許番号
US04882326

関連ノート

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