1,2-Dimethoxyethane → HCID 67241889, compound

HRID 1970394Notes

Reaction equation

HRID 1970394 reaction equation
C(=O)([O-])[O-].[Na+].[Na+].[N:7]1[CH:12]=[C:11](B(O)O)[CH:10]=[N:9][CH:8]=1.[Br:16][C:17]1[CH:30]=[CH:29][C:28]2[O:27][C:26]3[C:21](=[CH:22][C:23](I)=[CH:24][CH:25]=3)[C:20]3([CH2:35][S:34][C:33]([NH:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[N:32]3)[C:19]=2[CH:18]=1.COCCOC>CCOC(C)=O.O>[Br:16][C:17]1[CH:30]=[CH:29][C:28]2[O:27][C:26]3[C:21](=[CH:22][C:23]([C:11]4[CH:12]=[N:7][CH:8]=[N:9][CH:10]=4)=[CH:24][CH:25]=3)[C:20]3([CH2:35][S:34][C:33]([NH:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[N:32]3)[C:19]=2[CH:18]=1

Participants

7

Reactant 4

HCID 80711,2-DimethoxyethaneHCID 10340Sodium CarbonateHCID 2795193(Pyrimidin-5-yl)boronic acidHCID 67241916HCID 67241916, compound

Product 1

HCID 67241889HCID 67241889, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
80 °C

Procedure

To a mixture of sodium carbonate (1.562 g, 14.74 mmol), palladium tetrakistriphenylphosphine (0.454 g, 0.393 mmol), pyrimidin-5-ylboronic acid (0.791 g, 6.39 mmol) and 2′-bromo-N-tert-butyl-7′-iodo-5H-spiro[thiazole-4,9′-xanthen]-2-amine (2.600 g, 4.91 mmol) in a resealable pressure tube, was added DME (15 mL) and water (5 mL) at RT. The tube was sealed and heated to 80° C. After 24 hrs, the mixture was cooled to RT, diluted with EtOAc, and washed with water and brine. The organic fraction was adsorbed onto silica gel and purified by silica gel chromatography using 40% hexanes:EtOAc to afford 2′-bromo-N-tert-butyl-7′-(pyrimidin-5-yl)-5H-spiro[thiazole-4,9′-xanthen]-2-amine. MH+=481.0/483.0.

Workup

  1. customThe tube was sealed
  2. temperaturethe mixture was cooled to RT
  3. washwashed with water and brine
  4. custompurified by silica gel chromatography

Sources & evidence

ORD record
ord-261deae6891545be932a0a22036b76e0
Source dataset
uspto-grants-2013_04
Patent number
US08426447B2

Reaction notes

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