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HCID 86755670、化合物 → HCID 57090370、化合物

HRID 1872463
ノート
印刷プレビュー

反応式

HRID 1872463 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][CH2:26][CH:27]=[CH2:28])[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][CH2:26][CH2:27][CH3:28])[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 86755670HCID 86755670、化合物

生成物 1

HCID 57090370HCID 57090370、化合物収率 73.2%

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)-3-allyloxy-2-azido-bicyclo [3.1.0]hexane-2,6-dicarboxylic acid 2-benzyl ester 6-ethyl ester (XXIII-2) (28 mg, 0.073 mmol) in HOAc (0.75 mL) and H2O (0.25 mL) was hydrogenated in the presence of Pd/C (3 mg, 10% Pd/C) at 23° C. for 18 h. The catalyst was removed by filtration, the filter cake washed with 50% aqueous ethanol. After removal of the solvent in vacuum, the beige residue was refluxed in 10% HCl (1.25 mL) for 4 h. The solution was cooled to 23° C. and evaporated to dryness. The remaining pale yellow solid was dissolved in EtOH (1 mL) and propylene oxide (0.5 mL) and refluxed for 10 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-propoxy-bicyclo [3.1.0]hexane-2,6-dicarboxylic acid (I-8) (13 mg, 72%) as a white solid. 1H-NMR (250 MHz, D2O) □0.81 (1H, t, J=7.5 Hz), 1.48 (2H, m), 1.84 (1H, m), 2.16 (3H, m), 2.26 (1H, dd,J=12,7 Hz), 3.43 (2H, m), 3.73 (1H,bt,J=8Hz); MS[ISN] 242 [(M-H)- ]; mp >2500 C; □D20 3.72° (c=0.19, H2O).

後処理

  1. customThe catalyst was removed by filtration
  2. washthe filter cake washed with 50% aqueous ethanol
  3. customAfter removal of the solvent in vacuum
  4. temperaturethe beige residue was refluxed in 10% HCl (1.25 mL) for 4 h
  5. customevaporated to dryness
  6. dissolutionThe remaining pale yellow solid was dissolved in EtOH (1 mL)
  7. temperaturepropylene oxide (0.5 mL) and refluxed for 10 min, whereupon the amino acid
  8. temperatureAfter cooling to 23° C.
  9. filtrationthe product was filtered off
  10. washwashed with ether
  11. customdried

出典と根拠

ORDレコード
ord-38c5022b5cb34267bdb4b390f17bfee6
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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