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HCID 86755669、化合物 → HCID 57161051、化合物

HRID 1872462
ノート
印刷プレビュー

反応式

HRID 1872462 の反応式
C([O:3][C:4]([C@@H:6]1[C@@H:11]2[C@H:7]1[CH2:8][C@@H:9]([O:25][CH3:26])[C@@:10]2([N:22]=[N+]=[N-])[C:12]([O:14]CC1C=CC=CC=1)=[O:13])=[O:5])C>CC(O)=O.O.[Pd]>[NH2:22][C@@:10]1([C:12]([OH:14])=[O:13])[C@H:9]([O:25][CH3:26])[CH2:8][C@@H:7]2[C@H:11]1[C@H:6]2[C:4]([OH:5])=[O:3]
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

5

反応物 1

HCID 86755669HCID 86755669、化合物

生成物 1

HCID 57161051HCID 57161051、化合物収率 83%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒HCID 962Water溶媒

反応条件

温度
23 °C

実験手順

A solution of (1S,2R,3R,5R,6S)-2-azido-3-methoxy-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid 2-benzyl ester 6-ethyl ester (XXIII-1) (214 mg, 0.56 mmol) in HOAc (8 mL) and H2O (2 mL) was hydrogenated in the presence of Pd/C (35 mg, 10% Pd/C) at 23° C. for 18 h. The catalyst was removed by filtration, the filter cake washed with 50% aqueous acetic acid. After removal of the solvent in vacuum, the beige residue was refluxed in 10% HCl (15 mL) for 4 h. The solution was cooled to 23° C., filtered, washed with water and evaporated to dryness. The remaining pale yellow solid was dissolved in EtOH (10 mL) and propylene oxide (5.6 mL) and refluxed for 15 min, whereupon the amino acid precipiated. After cooling to 23° C., the product was filtered off, washed with ether and dried to give (1S,2R,3R,5R,6S)-2-amino-3-methoxy-bicyclo [3.1.0]hexane-2,6-dicarboxylic acid (I-7) (100 mg 74%) as a white solid. 1H-NMR (250 MHz, D2O) □1.86 (1H, t, J=3.5 Hz), 2.04-2.23 (3H, m), 2.50 (1H, dd, J=12, 7 Hz), 3.29 (3H, s), 3.62 (1H, bt,J=8 Hz); MS[ISN] 214 [(M-H)- ]; mp>250° C.; □D20 -13.84° (c=1.01, H2O).

後処理

  1. customThe catalyst was removed by filtration
  2. washthe filter cake washed with 50% aqueous acetic acid
  3. customAfter removal of the solvent in vacuum
  4. temperaturethe beige residue was refluxed in 10% HCl (15 mL) for 4 h
  5. filtrationfiltered
  6. washwashed with water
  7. customevaporated to dryness
  8. dissolutionThe remaining pale yellow solid was dissolved in EtOH (10 mL)
  9. temperaturepropylene oxide (5.6 mL) and refluxed for 15 min, whereupon the amino acid
  10. temperatureAfter cooling to 23° C.
  11. filtrationthe product was filtered off
  12. washwashed with ether
  13. customdried

出典と根拠

ORDレコード
ord-ed326366dbdc490497e13b32a1081d95
出典データセット
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06107342

反応ノート

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