Bromoacetic Acid → HCID 59430591, compound

HRID 502190Notes

Reaction equation

HRID 502190 reaction equation
Br[CH2:2][C:3]([OH:5])=O.CCN=C=NCCCN(C)C.[ClH:17].[NH2:18][C:19]1[CH:20]=[C:21]([C:26]2[N:27]([CH2:39][CH3:40])[C:28]3[C:33]([C:34]=2[C:35]#[N:36])=[CH:32][CH:31]=[C:30]([O:37][CH3:38])[CH:29]=3)[CH:22]=[CH:23][C:24]=1[OH:25]>C(#N)C>[Cl:17][CH2:2][C:3]([NH:18][C:19]1[CH:20]=[C:21]([C:26]2[N:27]([CH2:39][CH3:40])[C:28]3[C:33]([C:34]=2[C:35]#[N:36])=[CH:32][CH:31]=[C:30]([O:37][CH3:38])[CH:29]=3)[CH:22]=[CH:23][C:24]=1[OH:25])=[O:5]

Participants

5

Reactant 3

HCID 6227Bromoacetic AcidHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 59425699HCID 59425699, compound

Product 1

HCID 59430591HCID 59430591, compoundYield 64.7%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent2×

Procedure

Bromoacetic acid (52 mg, 0.37 mmol) is combined with EDCI hydrochloride (62 mg, 0.4 mmol) and acetonitrile (900 μL) to form a homogeneous solution. 2-(3-Amino-4-hydroxyphenyl)-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (100 mg, 0.33 mmol), prepared as in example 1BG, step B, is added to the solution. A thick paste soon forms. Another 1.1 mL of acetonitrile is added and the mixture is then stirred at room temperature for 2 hours. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is dried and concentrated. Purification by silica gel chromatography (4/1, CH2Cl2/EtOAc) yields 2-chloro-N-[5-(3-cyano-1-ethyl-6-methoxy-1H-indol-2-yl)-2-hydroxyphenyl]acetamide (82 mg, 60%), compound 333, as a white solid.

Workup

  1. customto form a homogeneous solution
  2. additionis added to the solution
  3. customThe reaction mixture is then partitioned between H2O and EtOAc
  4. customThe organic layer is dried
  5. concentrationconcentrated
  6. customPurification by silica gel chromatography (4/1, CH2Cl2/EtOAc)

Sources & evidence

ORD record
ord-4dc2dbcc205b4626aa431a6ef1b75863
Source dataset
uspto-grants-2010_08
Patent number
US07772271B2

Reaction notes

Loading…