Dimethylformamide → 4-Oxo-4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester

HRID 2237427Notes

Reaction equation

HRID 2237427 reaction equation
[CH2:1]([O:3][C:4]([N:6]([CH2:14][C:15]([OH:17])=O)[CH2:7][CH2:8][C:9]1[S:10][CH:11]=[CH:12][CH:13]=1)=[O:5])[CH3:2].CN(C=O)C.C(Cl)(=O)C(Cl)=O.[Al+3].[Cl-].[Cl-].[Cl-]>C(Cl)Cl>[CH2:1]([O:3][C:4]([N:6]1[CH2:14][C:15](=[O:17])[C:13]2[CH:12]=[CH:11][S:10][C:9]=2[CH2:8][CH2:7]1)=[O:5])[CH3:2]

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 59302576[Ethoxycarbonyl-(2-thiophen-2-yl-ethyl)-amino]-acetic acid

Product 1

HCID 574239834-Oxo-4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The product of step b) (˜165 mmol) was dissolved in 1 L of DCM. DMF (100 uL) was added followed slowly by oxalyl chloride (21.7 mL, 247 mmol). After 1 hour the reaction was concentrated to dryness and the crude material was re-dissolved in DCE (1 L). AlCl3 (55 g, 410 mmol) was carefully added and the reaction was stirred at room temperature for ½ hour. The crude reaction was quenched with ice, diluted with EtOH (300 mL), washed with water (3×), and dried over MgSO4. The title product was purified by silica gel chromatography (30% EtOAc in Hexanes) to give 10.5 g of the subtitle compound as an off-white solid. MS: ESI (positive): 240 (M+H).

Workup

  1. concentrationAfter 1 hour the reaction was concentrated to dryness
  2. dissolutionthe crude material was re-dissolved in DCE (1 L)
  3. customThe crude reaction
  4. customwas quenched with ice
  5. additiondiluted with EtOH (300 mL)
  6. washwashed with water (3×)
  7. dry with materialdried over MgSO4
  8. customThe title product was purified by silica gel chromatography (30% EtOAc in Hexanes)

Sources & evidence

ORD record
ord-362f41a10da74be396b5d9cf89ca0ec9
Source dataset
uspto-grants-2010_05
Patent number
US07718647B2

Reaction notes

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