Acetic Acid → HCID 54188068, compound

HRID 1383772Notes

Reaction equation

HRID 1383772 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([OH:15])[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C(O)(=O)C.[C:20]([O:24][C:25]([NH:27][C@@H:28]1[CH2:32][CH2:31][NH:30][CH2:29]1)=[O:26])([CH3:23])([CH3:22])[CH3:21].C([BH3-])#N.[Na+]>CO.CC(O)C.C(OCC)(=O)C>[C:20]([O:24][C:25]([NH:27][C@@H:28]1[CH2:32][CH2:31][N:30]([CH:11]2[CH2:12][CH2:13][C:8]([C:5]3[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=3)([OH:15])[CH2:9][CH2:10]2)[CH2:29]1)=[O:26])([CH3:23])([CH3:21])[CH3:22]

Participants

7

Reactant 4

HCID 176Acetic AcidHCID 1514397(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 5003444Sodium cyanoborohydrideHCID 223953644-(4-Fluorophenyl)-4-hydroxycyclohexan-1-one

Product 1

HCID 54188068HCID 54188068, compoundYield 56%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 22055037Isopropanol ethyl acetateSolvent

Procedure

To a solution of 4-(4-Fluorophenyl)-4-hydroxy-cyclohexanone (2.0 g, 9.6 mmol) and acetic acid (2.6 ml, 48 mmol) in methanol (60 Ml) was added (3R)-(+)-3-(tert-butoxycarbonyl amino) pyrrolidine (2.6 g, 14.4 mmol). After stirring for 2 hours at room temperature, sodium cyanoborohydride (1M in tetrahydrofuran, 14.4 ml, 14.4 mmol) was added dropwise. The reaction mixture was stirred for 45 minutes, concentrated, diluted with 10% potassium hydrogen sulfate and extracted twice with ether. The aqueous solution was sasified with 1N sodium hydroxide and extracted with ethyl acetate three times. Washing with brine, drying and solvent evaporation gave an oil. Flash chromatography (silica gel, 2-propanol-ethyl acetate, 4:96 increasing to 8:92) gave 4-(3-(3R)-tert-Butoxycarbonylamino-pyrrolidin-1-yl)-1-(4-fluorophenyl)-cyclohexanol (2.0 g, 56%); 1H NMR (CDCl13) δ 7.46(m, 2H), 7.02 (m, 2H), 4.89 (m, 1H), 4.18 (m, 1H), 2.94 (m, 1H), 2.71 (m, 2H), 2.42 (m, 1H), 2.26 (m, 1H), 2.13 (m, 1H), 1.83 (m, 9H), 1.63 (m, 1H), 1.44 (s, 9H),

Workup

  1. stirringThe reaction mixture was stirred for 45 minutes
  2. concentrationconcentrated
  3. additiondiluted with 10% potassium hydrogen sulfate
  4. extractionextracted twice with ether
  5. extractionextracted with ethyl acetate three times
  6. washWashing with brine
  7. customdrying
  8. customsolvent evaporation
  9. customgave an oil

Sources & evidence

ORD record
ord-33f3c36e55e64ed28ae907217392f475
Source dataset
uspto-grants-2001_07
Patent number
US06255315B1

Reaction notes

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