Sodium Iodide → HCID 59394061, compound

HRID 884591Notes

Reaction equation

HRID 884591 reaction equation
[CH:1]([NH2:4])([CH3:3])[CH3:2].[I-].[Na+].CS(O[CH2:12][C:13]1[CH:14]=[C:15]([NH:23][C:24]([N:26]2[C:34]3[C:29](=[CH:30][C:31]([O:35][C:36]4[C:37]5[CH2:45][CH2:44][N:43](C(OC(C)(C)C)=O)[CH2:42][C:38]=5[N:39]=[CH:40][N:41]=4)=[CH:32][CH:33]=3)[CH:28]=[CH:27]2)=[O:25])[CH:16]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:18]=1)(=O)=O>C(Cl)Cl>[CH:1]([NH:4][CH2:12][C:13]1[CH:14]=[C:15]([NH:23][C:24]([N:26]2[C:34]3[C:29](=[CH:30][C:31]([O:35][C:36]4[C:37]5[CH2:45][CH2:44][NH:43][CH2:42][C:38]=5[N:39]=[CH:40][N:41]=4)=[CH:32][CH:33]=3)[CH:28]=[CH:27]2)=[O:25])[CH:16]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:18]=1)([CH3:3])[CH3:2]

Participants

5

Reactant 3

HCID 5238Sodium IodideHCID 6363IsopropylamineHCID 59394300tert-Butyl 4-(1-(3-((methylsulfonyloxy)methyl)-5-(trifluoromethyl)phenylcarbamoyl)-1H-indol-5-yloxy)-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate

Product 1

HCID 59394061HCID 59394061, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of the above mixture (0.15 g, 0.227 mmol) in 3 mL of DCM, isopropyl amine (0.06 mL, 0.680 mmol) is added followed by sodium iodide (0.1 g, 0.68 mmol). After 45 min, LC-MS shows that tert-butyl 4-(1-(3-((methylsulfonyloxy)methyl)-5-(trifluoromethyl)phenylcarbamoyl)-1H-indol-5-yloxy)-5,6-dihydropyrido[3,4-d]pyrimidine-7 (8H)-carboxylate is converted to desired product and the tert-butyl 4-(1-(3-(chloromethyl)-5-(trifluoromethyl)phenylcarbamoyl)-1H-indol-5-yloxy)-5,6-dihydropyrido[3,4-d]pyrimidine-7 (8H)-carboxylate left over. To the reaction 3 mL (0.227 mmol) of isopropyl amine is added followed by NaI (0.1 g, 0.68 mmol) and the mixture is heated to 45° C. for 2 h. The solvent is then removed and the residue diluted with EtOAc, washed with H2O, brine and the organic layer dried over Na2SO4. Following concentration the residue is separated by FCC (25-100% EtOAc/heptane). This product is then treated with 60 mL of 50% TFA/DCM at rt for 1.5 h. After concentration the residue is separated by semi-prep HPLC (C-18; 10-100% I/H2O with 0.1% NH4OH) to provide the title compound. MS (ESI) m/z 525.2 (M+1); 1H NMR (400 MHz, DMSO-d6) δ ppm 10.33 (s, 1H), 8.40 (s, 1H), 8.27 (d, J=8.8 Hz, 1H), 8.13 (d, J=3.8 Hz, 1H), 7.95 (d, J=15.2 Hz, 2H), 7.38-7.52 (m, 2H), 7.11 (dd, J=9.0, 2.4 Hz, 1H), 6.78 (d, J=3.8 Hz, 1H), 3.81 (d, J=7.6 Hz, 4H), 3.03 (t, J=5.8 Hz, 2H), 2.68-2.79 (m, 3H), 1.03 (d, J=6.1 Hz, 6H).

Sources & evidence

ORD record
ord-3266e3495656481d9896374610d944bb
Source dataset
uspto-grants-2012_08
Patent number
US08242125B2

Reaction notes

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