1,2-Dichloroethane → HCID 22034100, compound
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
- washwash with saturated aq NaHCO3 (2×10 mL) and saturated aq brine (2×10 mL)
- customdry
- concentrationconcentrate in vacuo
Sources & evidence
- ORD record
- ord-5ce4c539ed5a459e9dd1ffe79d325f06
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506762B1
Reaction notes
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