Sodium Bicarbonate → HCID 66733042, compound

HRID 1184641Notes

Reaction equation

HRID 1184641 reaction equation
[Cl:1][C:2]1[CH:40]=[CH:39][C:5]2[N:6]([C:20](=[O:38])[C:21]3[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:36])[C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=4[CH3:35])=[CH:23][C:22]=3[CH3:37])[CH2:7][CH2:8][CH2:9][CH:10]([O:11][C:12]([CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])=[O:13])[C:4]=2[CH:3]=1.C(=O)([O-])O.[Na+:45]>CC(C)=O>[Cl:1][C:2]1[CH:40]=[CH:39][C:5]2[N:6]([C:20](=[O:38])[C:21]3[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:36])[C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=4[CH3:35])=[CH:23][C:22]=3[CH3:37])[CH2:7][CH2:8][CH2:9][CH:10]([O:11][C:12]([CH2:14][CH2:15][CH2:16][C:17]([O-:19])=[O:18])=[O:13])[C:4]=2[CH:3]=1.[Na+:45]

Participants

4

Reactant 2

HCID 516892Sodium BicarbonateHCID 66733043HCID 66733043, compound

Product 1

HCID 66733042HCID 66733042, compoundYield 45.2%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

4-{7-Chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yloxycarbonyl}butyric acid (0.30 g, 0.53 mmol) was dissolved in acetone (2 ml). A sodium hydrogen carbonate (45 mg, 0.53 mmol) aqueous solution (2 ml) was added thereto and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated, and the residue was washed with ethyl acetate and then air-dried to obtain 0.14 g (45%) of sodium 4-{7-chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yloxycarbonyl}butyrate as amorphous.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. washthe residue was washed with ethyl acetate
  3. customair-dried

Sources & evidence

ORD record
ord-bf4acea53a7a476a8c489f16bb50bef2
Source dataset
uspto-grants-2014_03
Patent number
US08669229B2

Reaction notes

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