HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Sodium Carbonate → Cyclopropyl-{5''-[4-(4-isopropyl-piperazin-1-ylmethyl)-phenyl]-[2,2';4',3'']terpyridin-6'-yl}-amine

HRID 1798487
Notes
Print preview

Reaction equation

HRID 1798487 reaction equation
[CH:1]([N:4]1[CH2:9][CH2:8][N:7]([CH2:10][C:11]2[CH:16]=[CH:15][C:14](B(O)O)=[CH:13][CH:12]=2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2].C([O-])([O-])=O.[Na+].[Na+].Br[C:27]1[CH:28]=[C:29]([C:33]2[CH:38]=[C:37]([NH:39][CH:40]3[CH2:42][CH2:41]3)[N:36]=[C:35]([C:43]3[CH:48]=[CH:47][CH:46]=[CH:45][N:44]=3)[CH:34]=2)[CH:30]=[N:31][CH:32]=1>COCCOC.C(Cl)Cl>[CH:40]1([NH:39][C:37]2[N:36]=[C:35]([C:43]3[CH:48]=[CH:47][CH:46]=[CH:45][N:44]=3)[CH:34]=[C:33]([C:29]3[CH:30]=[N:31][CH:32]=[C:27]([C:14]4[CH:15]=[CH:16][C:11]([CH2:10][N:7]5[CH2:8][CH2:9][N:4]([CH:1]([CH3:3])[CH3:2])[CH2:5][CH2:6]5)=[CH:12][CH:13]=4)[CH:28]=3)[CH:38]=2)[CH2:42][CH2:41]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 10340Sodium CarbonateHCID 44135953(5''-Bromo-[2,2';4',3'']terpyridin-6'-yl)-cyclopropyl-amineHCID 615342304-((4-Isopropyl-piperazin-1-yl)methyl)-phenyl boronic acid2×

Product 1

HCID 68759050Cyclopropyl-{5''-[4-(4-isopropyl-piperazin-1-ylmethyl)-phenyl]-[2,2';4',3'']terpyridin-6'-yl}-amine

Reagents, catalysts & solvents 2

HCID 6344
Dichloromethane
Solvent
HCID 80711,2-DimethoxyethaneSolvent

Procedure

To a solution of 4-((4-Isopropyl-piperazin-1-yl)methyl)-phenyl boronic acid (Intermediate B3) (3 eq, 0.408 mmol, 0.106 g) in dry DME (1 ml) under an inert atmosphere of argon is added 2M Na2CO3 (6 eq, 0.816 mmol, 0.8 ml) followed by (5″-Bromo-[2,2′;4′,3″]terpyridin-6′-yl)-cyclopropyl-amine (Example 1.26) (1 eq, 0.136 mmol, 50 mg) and PdCl2dppf (0.1 eq, 0.0136 mmol, 10 mg). The reaction mixture is heated using microwave radiation at 90° C. for 2 hours. The reaction mixture is dissolved in DCM and washed with water. The organic solvent is reduced in vacuo and the residue is purified by reverse phase column chromatography (Isolute™ C18, 0-40% acetonitrile in water—0.1% TFA). The appropriate fractions by HPLC are combined and concentrated in vacuo. The resulting residue is dissolved in MeOH and loaded onto a SCX-2 cartridge eluting with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions are combined, concentrated in vacuo and dried under vacuum to afford the title compound; [M+H]+ 505.

Workup

  1. temperatureThe reaction mixture is heated
  2. customat 90° C.
  3. customfor 2 hours
  4. washwashed with water
  5. customthe residue is purified by reverse phase column chromatography (Isolute™ C18, 0-40% acetonitrile in water—0.1% TFA)
  6. concentrationconcentrated in vacuo
  7. dissolutionThe resulting residue is dissolved in MeOH
  8. washeluting with MeOH
  9. concentrationconcentrated in vacuo
  10. customdried under vacuum

Sources & evidence

ORD record
ord-b9db4472f022418a952df79e5bcb1694
Source dataset
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08343966B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes