Hydrochloric Acid → 2-Fluoro-3-(piperidin-3-yl)pyridine dihydrochloride

HRID 1880145ノート

反応式

HRID 1880145 の反応式
[F:1][C:2]1[C:7]([C:8]2[CH2:9][CH2:10][CH2:11][N:12](C(OC(C)(C)C)=O)[CH:13]=2)=[CH:6][CH:5]=[CH:4][N:3]=1.[ClH:21].CC(O)C>[Pd].CCO>[ClH:21].[ClH:21].[F:1][C:2]1[C:7]([CH:8]2[CH2:9][CH2:10][CH2:11][NH:12][CH2:13]2)=[CH:6][CH:5]=[CH:4][N:3]=1

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 3776IsopropanolHCID 59326930tert-butyl 5-(2-fluoropyridin-3-yl)-3,4-dihydropyridine-1(2H)-carboxylate

生成物 1

HCID 674169432-Fluoro-3-(piperidin-3-yl)pyridine dihydrochloride

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a N2 purged round bottomed flask containing tert-butyl 5-(2-fluoropyridin-3-yl)-3,4-dihydropyridine-1(2H)-carboxylate (673 mg, 2.418 mmol) was added 10% Pd/C (50 mg, 0.470 mmol) and EtOH (15 mL). After stirring for 5 minutes, 5N HCl in iPrOH (4.0 mL, 20.00 mmol) was added and the flask capped with a balloon of H2. After 16 hours, LC-MS shows ˜30% conversion. The balloon was refilled. After a further 5 days, LC-MS shows complete consumption of starting material. The reaction was filtered through a celite cartridge and the cartridge rinsed with DCM:10% EtOH (50 mL). The filtrate was concentrated in vacuo to give 2-fluoro-3-(piperidin-3-yl)pyridine dihydrochloride as a yellow foam. The material was carried forward without further purification.

後処理

  1. customthe flask capped with a balloon of H2
  2. waitAfter 16 hours
  3. additionThe balloon was refilled
  4. waitAfter a further 5 days
  5. customconsumption of starting material
  6. filtrationThe reaction was filtered through a celite cartridge
  7. washthe cartridge rinsed with DCM
  8. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-4da4d93ebab64b97badafdbf328deecf
出典データセット
uspto-grants-2012_11
特許番号
US08318718B2

反応ノート

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