Triethylamine → HCID 178440277, compound

HRID 411579Notes

Reaction equation

HRID 411579 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[N:10]1[C:14]2=[N:15][C:16]([CH2:20][C:21]3[CH:26]=[CH:25][C:24]([NH2:27])=[CH:23][CH:22]=3)=[N:17][C:18](=[O:19])[C:13]2=[C:12]([CH:28]([CH3:30])[CH3:29])[NH:11]1.[C:31](N1CCC[C@H]1C(O)=O)([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32].C([N:48]([CH2:51][CH3:52])[CH2:49][CH3:50])C.C[CH2:54][O:55]C(C)=O>CN(C=O)C>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[N:10]1[C:14]2=[N:15][C:16]([CH2:20][C:21]3[CH:26]=[CH:25][C:24]([N:27]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[C:54](=[O:55])[C@@H:51]4[CH2:52][CH2:50][CH2:49][NH:48]4)=[CH:23][CH:22]=3)=[N:17][C:18](=[O:19])[C:13]2=[C:12]([CH:28]([CH3:30])[CH3:29])[NH:11]1

Participants

6

Procedure

To a stirred solution of 105 mg (0.22 mmol) of 1-(2,4,6-trichlorophenyl)-3-isopropyl-6-(4-aminobenzyl)pyrazolo[3,4-d]pyrimidin-4-one and 235 mg (1.09 mmol) of Boc-L-proline in 2 mL of DMF was added 0.35 mL (2.5 mmol) of triethylamine followed by 490 mg (1.11 mmol) of Bop. The solution was stirred overnight at ambient temperature then poured into EtOAc. This solution was washed sequentally with 0.5 M HCl then dilute aq. Na2CO3 then brine, dried (MgSO4), and concentrated under reduced pressure. The crude product was recrystallized from EtOAc-hexanes to afford 116 mg (80%) of (S)-1-(2,4,6-trichlorophenyl)-3-isopropyl-6-(4-(N-t-butoxycarbonylprolinamido)benzyl)pyrazolo[3,4-d]pyrimidin-4-one as a white solid, mp 225-226° C., Mass spec.: 657 M−H−).

Workup

  1. washThis solution was washed sequentally with 0.5 M HCl
  2. dry with materialdilute aq. Na2CO3 then brine, dried (MgSO4)
  3. concentrationconcentrated under reduced pressure
  4. customThe crude product was recrystallized from EtOAc-hexanes

Sources & evidence

ORD record
ord-d269b0db8f8948c1a5ef469d4a56177c
Source dataset
uspto-grants-2003_05
Patent number
US06559152B2

Reaction notes

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