Triethylamine → HCID 24948782, compound

HRID 1783797Notes

Reaction equation

HRID 1783797 reaction equation
[CH:1]1[CH:6]=[C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([NH2:11])[C:4]2=[CH:3][CH:2]=1.C(N(CC)CC)C.Cl.[N:20]1([CH2:26][CH2:27][C:28]2[N:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]3=[C:30]([C:37](Cl)=[O:38])[N:29]=2)[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1>C(Cl)Cl>[C:10]1([NH:11][C:37]([C:30]2[N:29]=[C:28]([CH2:27][CH2:26][N:20]3[CH2:21][CH2:22][O:23][CH2:24][CH2:25]3)[N:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]=23)=[O:38])[C:4]2[C:5](=[CH:6][CH:1]=[CH:2][CH:3]=2)[CH:7]=[CH:8][CH:9]=1

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 86401-NaphthylamineHCID 86617456HCID 86617456, compound

Product 1

HCID 24948782HCID 24948782, compoundYield 32.2%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 1-naphylamine (0.077 g, 0.54 mmol) and triethylamine (0.16 mL, 1.14 mmol) in CH2Cl2 (10 mL) was added 3-(2-morpholin-4-yl-ethyl)-imidazo[1,5-a]pyridine-1-carbonyl chloride hydrochloride (150 mg, 0.45 mmol). The mixture was stirred at ambient temperature for 1 h then washed with sat. aq. NaHCO3 (20 mL). The organic layer was separated and the aqueous layer was extracted with dichloromethane (20 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was chromatographed on silica to yield the title compound (58 mg, 32%). 1H NMR (DMSO-d6) δ 10.0 (1H), 8.45 (1H), 8.10 (1H), 7.98 (3H), 7.78 (1H), 7.55 (3H), 7.18 (1H), 6.93 (1H), 3.59 (4H), 3.30 (2H), 2.85 (2H), 2.57 (4H); m/z (M+H)=401.13.

Workup

  1. washthen washed with sat. aq. NaHCO3 (20 mL)
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with dichloromethane (20 mL)
  4. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue was chromatographed on silica

Sources & evidence

ORD record
ord-0d66ee03b78c44c5bb4aabb7d442f349
Source dataset
uspto-grants-2009_03
Patent number
US07501438B2

Reaction notes

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