Water → HCID 56943217, compound

HRID 1631148Notes

Reaction equation

Br[C:2]1[CH:14]=[C:13]([F:15])[C:12]([F:16])=[CH:11][C:3]=1[CH2:4][N:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[CH3:6].C(=O)([O-])[O-].[K+].[K+].O.[NH2:24][C:25]1[N:34]=[C:33]([C:35]([N:37]2[CH2:45][C:44]3[C:39](=[CH:40][CH:41]=[CH:42][CH:43]=3)[CH2:38]2)=[O:36])[C:32]2[C:27](=[CH:28][CH:29]=[C:30](B3OC(C)(C)C(C)(C)O3)[CH:31]=2)[N:26]=1>C(O)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[NH2:24][C:25]1[N:34]=[C:33]([C:35]([N:37]2[CH2:38][C:39]3[C:44](=[CH:43][CH:42]=[CH:41][CH:40]=3)[CH2:45]2)=[O:36])[C:32]2[C:27](=[CH:28][CH:29]=[C:30]([C:2]3[CH:14]=[C:13]([F:15])[C:12]([F:16])=[CH:11][C:3]=3[CH2:4][N:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[CH3:6])[CH:31]=2)[N:26]=1

Participants

Conditions

Temperature: 120 °C

Procedure

171 mg of (2-bromo-4,5-difluorobenzyl)-tert-butylmethylamine, 124 mg of potassium carbonate, 9 μl of water and 22 mg of [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride are added to a solution of 150 mg of [2-amino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinazolin-4-yl]-(1,3-dihydroisoindol-2-yl)methanone in 4 ml of ethanol under argon. The mixture is heated at 120° C. for 30 min; the hot mixture is filtered through kieselguhr, and the filtrate is evaporated. and purified by chromatography (reversed phase HPLC).

Workup

filtrationthe hot mixture is filtered through kieselguhr
customthe filtrate is evaporated
customand purified by chromatography (reversed phase HPLC)

Sources & evidence

ORD record: ord-b826d44cf376494b8739b0e35b8a052f
Source dataset: uspto-grants-2014_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08791129B2

Reaction notes

Loading…