2-(4-Methoxy-3-nitro-benzoylamino)-indane-2-carboxylic acid methyl ester → HCID 67076603, compound

HRID 2405237Notes

Reaction equation

HRID 2405237 reaction equation
[CH3:1][O:2][C:3]([C:5]1([NH:14][C:15](=[O:27])[C:16]2[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[C:18]([N+:24]([O-])=O)[CH:17]=2)[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)=[O:4]>CO.[Pd]>[CH3:1][O:2][C:3]([C:5]1([NH:14][C:15](=[O:27])[C:16]2[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[C:18]([NH2:24])[CH:17]=2)[CH2:6][C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH2:13]1)=[O:4]

Participants

4

Reactant 1

HCID 670766712-(4-Methoxy-3-nitro-benzoylamino)-indane-2-carboxylic acid methyl ester

Product 1

HCID 67076603HCID 67076603, compoundYield 96.2%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

The compound of step 1 (0.43 g, 1.16 mmol) was dissolved in methanol (30 ml), 10% palladium on charcoal (200 mg) was added, and the flask flushed with argon. A balloon filled with hydrogen was connected, and the mixture was stirred at room temperature overnight. The balloon was removed, the flask flushed with argon, the catalyst filtered off over Celite, and the filtrate was evaporated in vacuo to give 0.38 g of the title compound.

Workup

  1. customthe flask flushed with argon
  2. additionA balloon filled with hydrogen
  3. customThe balloon was removed
  4. customthe flask flushed with argon
  5. filtrationthe catalyst filtered off over Celite
  6. customthe filtrate was evaporated in vacuo

Sources & evidence

ORD record
ord-6eb00fcbeebb4b6bb121a29b55caa8ba
Source dataset
uspto-grants-2014_08
Patent number
US08802720B2

Reaction notes

Loading…