1,2-Dichloroethane → HCID 22034100, compound

HRID 1634569Notes

Reaction equation

HRID 1634569 reaction equation
[CH3:1][C:2]1[C:3]([O:14][C:15]2[C:20]([CH3:21])=[CH:19][C:18]([CH3:22])=[CH:17][C:16]=2[CH3:23])=[N:4][C:5]([CH3:13])=[CH:6][C:7]=1[NH:8][CH2:9][CH2:10][NH:11]C.[CH3:24][O:25][C:26]1[CH:27]=[C:28]([CH2:34][C:35]([OH:37])=O)[CH:29]=[CH:30][C:31]=1[O:32][CH3:33].C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1>CN(C=O)C.CCOC(C)=O>[CH3:24][O:25][C:26]1[CH:27]=[C:28]([CH2:34][C:35]([NH:11][CH2:10][CH2:9][NH:8][C:7]2[CH:6]=[C:5]([CH3:13])[N:4]=[C:3]([O:14][C:15]3[C:20]([CH3:21])=[CH:19][C:18]([CH3:22])=[CH:17][C:16]=3[CH3:23])[C:2]=2[CH3:1])=[O:37])[CH:29]=[CH:30][C:31]=1[O:32][CH3:33]

Participants

7

Procedure

Stir a solution of [3,6-dimethyl-2-(2,4,6-trimethyl-phenoxy)-4-pyridyl][2-(methylamino)ethyl]amine (68 mg, 0.23 mmol), 3,4-dimethoxyphenylacetic acid (59 mg, 0.3 mmol), EDC (59 mg, 0.3 mmol) and HOBT (41 mg, 0.3 mmol) in DMF (1.0 mL) for 12 h. Dilute the reaction mixture with EtOAc (10 mL) and wash with saturated aq NaHCO3 (2×10 mL) and saturated aq brine (2×10 mL), dry and concentrate in vacuo to obtain the title compound as an oily residue. M+1: 478.

Workup

  1. washwash with saturated aq NaHCO3 (2×10 mL) and saturated aq brine (2×10 mL)
  2. customdry
  3. concentrationconcentrate in vacuo

Sources & evidence

ORD record
ord-5ce4c539ed5a459e9dd1ffe79d325f06
Source dataset
uspto-grants-2003_01
Patent number
US06506762B1

Reaction notes

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