Propanamide, N,N-dimethyl- → HCID 86658860, compound

HRID 2194911Notes

Reaction equation

HRID 2194911 reaction equation
[Cl:1][C:2]1[CH:44]=[C:43]([CH3:45])[CH:42]=[C:41]([Cl:46])[C:3]=1[O:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH:15]([C:25]2[CH:30]=[CH:29][C:28](B3OC(C)(C)C(C)(C)O3)=[CH:27][C:26]=2[CH3:40])[CH2:16][NH:17][C:18](=[O:24])[O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[CH:10][CH:9]=1.[CH3:47][N:48]([CH3:53])[C:49](=[O:52])[CH2:50][CH3:51]>>[Cl:46][C:41]1[CH:42]=[C:43]([CH3:45])[CH:44]=[C:2]([Cl:1])[C:3]=1[O:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[CH:10][C:11]([CH2:14][CH:15]([C:25]2[CH:30]=[CH:29][C:28]([C:2]3[CH:44]=[CH:43][CH:42]=[CH:41][C:3]=3[CH2:51][CH2:50][C:49]([N:48]([CH3:53])[CH3:47])=[O:52])=[CH:27][C:26]=2[CH3:40])[CH2:16][NH:17][C:18](=[O:24])[O:19][C:20]([CH3:22])([CH3:23])[CH3:21])=[CH:12][CH:13]=1

Participants

3

Reactant 2

HCID 12965Propanamide, N,N-dimethyl-HCID 86658858HCID 86658858, compound

Product 1

HCID 86658860HCID 86658860, compound

Procedure

Prepared according to the procedure described in EXAMPLE 7, step 2 using tert-butyl {3-{4-[2-(2,6-dichloro-4-methylphenoxy)ethoxy]phenyl}-2-[2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propyl}carbamate from EXAMPLE 9, step 1 and 342-bromophenyl)-N,N-dimethylpropanamide (V.12) as starting materials. Purification by column chromatography on silica gel (Combi-Flash by ISCO), eluting with Hex/EtOAc (10 to 75% in 30 min) afforded the desired compound as a colorless oil.

Workup

  1. customPrepared
  2. customPurification by column chromatography on silica gel (Combi-Flash by ISCO)
  3. washeluting with Hex/EtOAc (10 to 75% in 30 min)

Sources & evidence

ORD record
ord-6cedd570da70485f96a26552fb4a8168
Source dataset
uspto-grants-2012_12
Patent number
US08334308B2

Reaction notes

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