Potassium Phosphate, Tribasic → HCID 56968749, compound

HRID 1047020Notes

Reaction equation

HRID 1047020 reaction equation
Br[C:2]1[N:3]=[C:4]2[C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=3[NH:8][C:7]3[N:15]=[CH:16][CH:17]=[CH:18][C:6]=3[N:5]2[C:19]=1[C:20]1[CH:25]=[CH:24][C:23]([C:26]2([NH:30]C(=O)OC(C)(C)C)[CH2:29][CH2:28][CH2:27]2)=[CH:22][CH:21]=1.[N:38]1[C:47]2[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=2)[CH:41]=[C:40](B(O)O)[CH:39]=1.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>CN(C=O)C.O.CCOC(C)=O.CC(P(C(C)(C)C)C1C=CC(N(C)C)=CC=1)(C)C.CC(P(C(C)(C)C)C1C=CC(N(C)C)=CC=1)(C)C.Cl[Pd]Cl>[N:38]1[C:47]2[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=2)[CH:41]=[C:40]([C:2]2[N:3]=[C:4]3[C:10]4[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=4[NH:8][C:7]4[N:15]=[CH:16][CH:17]=[CH:18][C:6]=4[N:5]3[C:19]=2[C:20]2[CH:25]=[CH:24][C:23]([C:26]3([NH2:30])[CH2:29][CH2:28][CH2:27]3)=[CH:22][CH:21]=2)[CH:39]=1

Participants

7

Reactant 3

HCID 62657Potassium Phosphate, TribasicHCID 2734663Quinoline-3-boronic acidHCID 136331865tert-butyl {1-[4-(2-bromo-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-3-yl)phenyl]cyclobutyl}carbamate

Product 1

HCID 56968749HCID 56968749, compoundYield 65.8%

Reagents, catalysts & solvents 3

HCID 11714597Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)CatalystHCID 8857Ethyl AcetateSolventHCID 21962138N,N-Dimethylformamide--water (1/1)Solvent

Conditions

Temperature
160 °C

Procedure

A mixture of tert-butyl {1-[4-(2-bromo-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-3-yl)phenyl]cyclobutyl}carbamate (50 mg, 0.09 mmol), quinolin-3-ylboronic acid (31 mg, 0.18 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (6.3 mg, 0.01 mmol) and K3PO4 (72 mg, 0.27 mmol) in DMF/water (0.9 mL, 6:1, v/v) was heated at 160° C. under microwave irradiation for 1 hour. After cooling to room temperature, the mixture was diluted with EtOAc and washed with water (×3). The organic layer was dried over anhydrous Na2SO4 and concentrated. The residue was purified by HPLC. To the fraction, conc. HCl (3 ml) and methanol (3 ml) were added and the residue was evaporated after 24 h. The residue was purified by HPLC to give the titled compound as a white solid (30 mg, 55%). 1HNMR (DMSO-d6) 400 MHz δ: 8.85 (d, J=2.3 Hz, 1H), 8.63 (s, 1H), 8.48 (d, J=2.3 Hz, 1H), 8.24 (s, 1H), 8.11 (dd, J=4.6, 1.7 Hz, 1H), 8.03 (dd, J=8.0, 1.7 Hz, 1H), 7.96 (d, J=8.6 Hz, 1H), 7.93 (d, J=7.4 Hz, 1H), 7.73 (t, J=7.4 Hz, 1H), 7.60 (t, J=7.4 Hz, 1H), 7.53 (d, J=8.6 Hz, 2H), 7.38 (t, J=8.6 Hz), 7.31 (d, J=7.4 Hz, 1H), 7.29 (d, J=8.0 Hz, 2H), 7.15 (t, J=8.0 Hz, 1H), 6.96 (dd, J=8.0, 1.7 Hz, 1H), 6.77 (dd, J=8.0, 4.6 Hz, 1H), 2.47-2.41 (m, 2H), 2.24-2.17 (m, 2H), 2.10-2.02 (m, 1H), 1.77-1.68 (m, 1H); LCMS: 507 [M+H].

Workup

  1. temperatureAfter cooling to room temperature
  2. washwashed with water (×3)
  3. dry with materialThe organic layer was dried over anhydrous Na2SO4
  4. concentrationconcentrated
  5. customThe residue was purified by HPLC
  6. additionTo the fraction, conc. HCl (3 ml) and methanol (3 ml) were added
  7. customthe residue was evaporated after 24 h
  8. customThe residue was purified by HPLC

Sources & evidence

ORD record
ord-1062a132f3ae48739b3c2e6f14d53a8e
Source dataset
uspto-grants-2013_10
Patent number
US08569331B2

Reaction notes

Loading…