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Phosgene → (S)-1-[[(S)-3-[[(Phenylmethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]carbonyl]-2-azetidinecarboxylic acid, phenylmethyl ester

HRID 482932
ノート
印刷プレビュー

反応式

HRID 482932 の反応式
[C:1]1([CH2:7][O:8][C:9]([NH:11][C@H:12]2[CH2:15][NH:14][C:13]2=[O:16])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(N(CC)CC)C.[C:24](Cl)(Cl)=[O:25].Cl.[NH:29]1[CH2:32][CH2:31][CH:30]1[C:33]([O:35][CH2:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)=[O:34].P([O-])([O-])([O-])=O.[K+].[K+].[K+]>ClCCl>[C:1]1([CH2:7][O:8][C:9]([NH:11][C@H:12]2[CH2:15][N:14]([C:24]([N:29]3[CH2:32][CH2:31][C@H:30]3[C:33]([O:35][CH2:36][C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=3)=[O:34])=[O:25])[C:13]2=[O:16])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 6371PhosgeneHCID 8471Triethylamine2 回HCID 62657Potassium Phosphate, TribasicHCID 12834624benzyl N-[(3S)-2-oxoazetidin-3-yl]carbamateHCID 70081492Azetidine-2-carboxylic acid, benzyl ester hydrochloride

生成物 1

HCID 86740685
(S)-1-[[(S)-3-[[(Phenylmethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]carbonyl]-2-azetidinecarboxylic acid, phenylmethyl ester

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-5 °C

実験手順

A slurry of (S)-3-[[(phenylmethoxy)carbonyl]amino]-2-azetidinone (0.78 g, 3.54 mmole) in dry dichloromethane was warmed briefly to 50° C. and then cooled to -5° C. Triethylamine (0.354 g, 3.54 mmole) and phosgene (5.7 ml of 12.5% phosgene/toluene) were added and the reaction was stirred at -5° C. for 2 hours. The reaction was concentrated to a residue and fresh dichloromethane was added. After the solution was cooled to -50° C., triethylamine (0.714 g, 7.08 mmole) and azetidine-2-carboxylic acid, benzyl ester hydrochloride (0.8 g, 3.54 mmole) were added. The reaction was stirred at -5° C. for 45 minutes. The reaction mixture was poured into 10% monobasic potassium phosphate and the dichloromethane layer was separated and washed with water and brine. After drying over sodium sulfate the solvent evaporated. The crude oil was flash chromatographed on silica (LPS-1) eluting with ethyl/acetate:hexane (1:1). Fractions containing pure compound were concentrated to give 0.622 g of the title compound.

後処理

  1. concentrationThe reaction was concentrated to a residue and fresh dichloromethane
  2. additionwas added
  3. temperatureAfter the solution was cooled to -50° C.
  4. stirringThe reaction was stirred at -5° C. for 45 minutes
  5. customthe dichloromethane layer was separated
  6. washwashed with water and brine
  7. dry with materialAfter drying over sodium sulfate the solvent
  8. customevaporated
  9. customchromatographed on silica (LPS-1)
  10. washeluting with ethyl/acetate
  11. additionFractions containing pure compound
  12. concentrationwere concentrated

出典と根拠

ORDレコード
ord-3f6fd980ca1f400faa0f9cb04919036e
出典データセット
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04576749

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート