Benzaldehyde → (+/-)-tert-butyl ((1R,2S,3S,5R)-5-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-3-methyl-2-(methylamino)cyclohexyl)carbamate

HRID 705303

反応式

HRID 705303 の反応式
[C:1]([O:5][C:6]([NH:8][C:9]1[CH:10]=[N:11][CH:12]=[CH:13][C:14]=1[C@H:15]1[CH2:20][C@@H:19]([NH:21][C:22](=[O:28])[O:23][C:24]([CH3:27])([CH3:26])[CH3:25])[C@@H:18]([NH2:29])[C@@H:17]([CH3:30])[CH2:16]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH:31](=O)C1C=CC=CC=1.[B-]C#N.[Na+].C=O>CO.[OH-].[OH-].[Pd+2]>[C:1]([O:5][C:6]([NH:8][C:9]1[CH:10]=[N:11][CH:12]=[CH:13][C:14]=1[C@H:15]1[CH2:20][C@@H:19]([NH:21][C:22](=[O:28])[O:23][C:24]([CH3:27])([CH3:26])[CH3:25])[C@@H:18]([NH:29][CH3:31])[C@@H:17]([CH3:30])[CH2:16]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

参加物

7

反応物 4

HCID 240BenzaldehydeHCID 712FormaldehydeHCID 20587905Sodium cyanoborohydride [MI]2 回HCID 86705267(+/-)-tert-butyl ((1R,2S,3S,5R)-5-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-2-amino-3-methylcyclohexyl)carbamate

生成物 1

HCID 86705268(+/-)-tert-butyl ((1R,2S,3S,5R)-5-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-3-methyl-2-(methylamino)cyclohexyl)carbamate収率 75%

試薬・触媒・溶媒 2

HCID 9942167Palladium hydroxide触媒HCID 887Methanol溶媒

実験手順

To a solution of (+/−)-tert-butyl ((1R,2S,3S,5R)-5-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-2-amino-3-methylcyclohexyl)carbamate (1.0 equiv.) in MeOH (0.10 M) was added benzaldehyde (1.3 equiv.). After 3 hrs, sodium cyanotrihydroborate (2.5 equiv.) was added and the mixture was stirred at rt for 16 hrs. The reaction mixture was quenched by the addition of water, and volatiles were removed in vacuo. The mixture was extracted with ethyl acetate. The combined organic phases were dried with sodium sulfate, filtered and concentrated. The residue was dissolved in MeOH (0.10 M) and paraformaldehyde (5.0 equiv.) was added. After 16 hrs, sodium cyanotrihydroborate (5.0 equiv.) was added and the mixture was left stirred at rt for 16 hrs. The reaction was quenched by the addition of water, and volatiles were removed in vacuo. The mixture was extracted with DCM. The combined organic phases were dried with sodium sulfate, filtered, concentrated and purified by ISCO Chromatography. The product was dissolved in MeOH (0.10 M) and treated with Pd(OH)2 (0.50 equiv.) under H2 for 5 hrs at RT. The reaction was filtered through a pad of celite and the cake was washed with MeOH. The organics were concentrated to yield (+/−)-tert-butyl ((1R,2S,3S,5R)-5-(3-((tert-butoxycarbonyl)amino)pyridin-4-yl)-3-methyl-2-(methylamino)cyclohexyl)carbamate in 75% yield. LC/MS (m/z)=435.2 (MH+), Rt=0.64 min.

後処理

  1. customThe reaction mixture was quenched by the addition of water, and volatiles
  2. customwere removed in vacuo
  3. extractionThe mixture was extracted with ethyl acetate
  4. dry with materialThe combined organic phases were dried with sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. dissolutionThe residue was dissolved in MeOH (0.10 M)
  8. waitAfter 16 hrs
  9. waitthe mixture was left
  10. stirringstirred at rt for 16 hrs
  11. customThe reaction was quenched by the addition of water, and volatiles
  12. customwere removed in vacuo
  13. extractionThe mixture was extracted with DCM
  14. dry with materialThe combined organic phases were dried with sodium sulfate
  15. filtrationfiltered
  16. concentrationconcentrated
  17. custompurified by ISCO Chromatography
  18. dissolutionThe product was dissolved in MeOH (0.10 M)
  19. filtrationThe reaction was filtered through a pad of celite
  20. washthe cake was washed with MeOH
  21. concentrationThe organics were concentrated

出典と根拠

ORDレコード
ord-d08c125a1f174bd39ffcf4b01d690e00
出典データセット
uspto-grants-2015_11
特許番号
US09173883B2

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