Diisopropylethylamine → HCID 178444812, compound

HRID 2243873Notes

Reaction equation

HRID 2243873 reaction equation
[C:1]([O:5][C:6](=[O:42])[NH:7][C:8](=[N:23][C:24](=[O:41])[CH2:25][C:26]([C:31]1[CH:36]=[CH:35][C:34]([O:37][CH2:38][CH:39]=[CH2:40])=[CH:33][CH:32]=1)=[N:27][O:28][CH2:29][CH3:30])[CH2:9][C:10]1[CH:15]=[C:14]([Cl:16])[C:13]([NH:17][C:18](=[O:21])[CH2:19]Br)=[C:12]([Cl:22])[CH:11]=1)([CH3:4])([CH3:3])[CH3:2].Cl.[CH2:44]([NH2:49])[CH2:45][CH2:46][CH:47]=[CH2:48].[CH:50](N(C(C)C)CC)(C)C>ClCCl>[C:1]([O:5][C:6](=[O:42])[NH:7][C:8](=[N:23][C:24](=[O:41])[CH2:25][C:26]([C:31]1[CH:36]=[CH:35][C:34]([O:37][CH2:38][CH:39]=[CH2:40])=[CH:33][CH:32]=1)=[N:27][O:28][CH2:29][CH3:30])[CH2:9][C:10]1[CH:15]=[C:14]([Cl:16])[C:13]([NH:17][C:18](=[O:21])[CH2:19][NH:49][CH2:44][CH2:45][CH2:46][CH2:47][CH:48]=[CH2:50])=[C:12]([Cl:22])[CH:11]=1)([CH3:4])([CH3:3])[CH3:2]

Participants

5

Reactant 3

HCID 81531DiisopropylethylamineHCID 46942242Pent-4-en-1-amine hydrochlorideHCID 178458368HCID 178458368, compound

Product 1

HCID 178444812HCID 178444812, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of tert-butyl-1-(3-(4-(allyloxy)phenyl)-3-(ethoxyimino)-propanoylimino)-2-(4-(2-bromoacetamido)-3,5-dichlorophenyl)ethylcarbamate (60 mg) in dichloromethane (0.30 mL) at room temperature was added pent-4-en-1-amine hydrochloride (47 mg) and diisopropylethylamine (76 μL), and the resulting solution was stirred at room temperature for 4 h. The solvents were removed in vacuo to give the title compound as a white solid, which was used in Step B without purification. retention time: 2.10 min (method A). MS (ESI) (M+H)+ 717.83.

Workup

  1. customThe solvents were removed in vacuo

Sources & evidence

ORD record
ord-036646df7f53440d80d6fc031209c635
Source dataset
uspto-grants-2010_03
Patent number
US07678784B2

Reaction notes

Loading…