Methanol → HCID 58999602, compound

HRID 1593591Notes

Reaction equation

HRID 1593591 reaction equation
[C:1]12([CH2:11][NH:12][C:13]([C:15]3[C:16]4[CH2:24][CH2:23][N:22](CC5C=CC=CC=5)[CH2:21][C:17]=4[N:18]=[CH:19][N:20]=3)=[O:14])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.C(Cl)Cl.CO>C(O)(=O)C.[Pd]>[C:1]12([CH2:11][NH:12][C:13]([C:15]3[C:16]4[CH2:24][CH2:23][NH:22][CH2:21][C:17]=4[N:18]=[CH:19][N:20]=3)=[O:14])[CH2:8][CH:7]3[CH2:9][CH:3]([CH2:4][CH:5]([CH2:6]3)[CH2:10]1)[CH2:2]2

Participants

6

Procedure

In a round bottom flask, 7-Benzyl-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimdine-4-carboxylic acid(adamantan-1-ylmethyl)-amide(1.15 g, 2.74 mmol) was dissolved in glacial acetic acid (10 mL) with stirring and 10% Pd/C (417 mg) was added. The suspension was stirred under an atmosphere of H2 for 16 h. By LCMS and TLC (DCM:MeOH::20:1), no starting material appeared to be present. The desired m/z was observed at 327.3 (M+H). The reaction mixture was then filtered through a pad of celite. The filtrate was concentrated. The resulting oil was re-dissolved in EtOAc (50 mL) with stirring. A 10% NaOH solution (50 mL) was added. The mixture was stirred at RT for 1 h. The layers were separated and the aqueous layer was extracted with EtOAc (3×50 mL). The combined organic layers were filtered through a Horizon Technologies DryDisk and concentrated. The crude oil was chromatographed using DCM/MeOH (0-30% gradient) as elutant affording 0.133 g of the title compound.

Workup

  1. stirringThe suspension was stirred under an atmosphere of H2 for 16 h
  2. filtrationThe reaction mixture was then filtered through a pad of celite
  3. concentrationThe filtrate was concentrated
  4. dissolutionThe resulting oil was re-dissolved in EtOAc (50 mL)
  5. stirringwith stirring
  6. additionA 10% NaOH solution (50 mL) was added
  7. stirringThe mixture was stirred at RT for 1 h
  8. customThe layers were separated
  9. extractionthe aqueous layer was extracted with EtOAc (3×50 mL)
  10. filtrationThe combined organic layers were filtered through a Horizon Technologies DryDisk
  11. concentrationconcentrated
  12. customThe crude oil was chromatographed

Sources & evidence

ORD record
ord-2f402f2b27e54e3fb2368c8c790b6a95
Source dataset
uspto-grants-2007_11
Patent number
US07297700B2

Reaction notes

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