Boron tribromide → HCID 11475767, compound

HRID 1443152Notes

Reaction equation

HRID 1443152 reaction equation
[F:1][C:2]1[C:11]([O:12]C)=[CH:10][CH:9]=[C:8]2[C:3]=1[C:4]([CH3:31])([CH3:30])[CH2:5][C:6]([OH:29])([C:25]([F:28])([F:27])[F:26])[CH:7]2[NH:14][C:15]1[CH:23]=[CH:22][CH:21]=[C:20]2[C:16]=1[CH2:17][NH:18][C:19]2=[O:24].B(Br)(Br)Br.C(=O)(O)[O-].[Na+]>ClCCl>[F:1][C:2]1[C:11]([OH:12])=[CH:10][CH:9]=[C:8]2[C:3]=1[C:4]([CH3:31])([CH3:30])[CH2:5][C:6]([OH:29])([C:25]([F:27])([F:28])[F:26])[CH:7]2[NH:14][C:15]1[CH:23]=[CH:22][CH:21]=[C:20]2[C:16]=1[CH2:17][NH:18][C:19]2=[O:24]

Participants

5

Reactant 3

HCID 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 68680359HCID 68680359, compound

Product 1

HCID 11475767HCID 11475767, compoundYield 14.7%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

109.8 mg (0.250 mmol) of (rac.) 4-{[5-fluoro-2-hydroxy-6-methoxy-4,4-dimethyl-2-(trifluoromethyl)-1,2,3,4-tetrahydronaphthalen-1-yl]amino}-2,3-dihydroisoindol-1-one is mixed with 3.4 ml of a 1 M solution of BBr3 in dichloromethane and stirred for four hours at room temperature. The batch is mixed at 0° C. with saturated sodium bicarbonate solution and extracted twice with ethyl cetate. The combined organic extracts are dried on sodium sulfate. After the desiccant is filtered off, and after the solvent is spun off, the residue is chromatographed on a Flashmaster. 15.6 mg (14.7%) of the final product is isolated.

Workup

  1. extractionextracted twice with ethyl cetate
  2. customThe combined organic extracts are dried on sodium sulfate
  3. filtrationAfter the desiccant is filtered off
  4. customthe residue is chromatographed on a Flashmaster

Sources & evidence

ORD record
ord-f46127722b38421891db15dc0de14e11
Source dataset
uspto-grants-2010_02
Patent number
US07659297B2

Reaction notes

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