Dichloromethane → Ammonium Hydroxide

HRID 1594861Notes

Reaction equation

HRID 1594861 reaction equation
[C:1]([O:5][C:6](=[O:26])[NH:7][CH2:8][CH2:9][C:10]1[N:11]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[C:19](F)[CH:18]=2)[C:12]([CH3:15])=[N:13][CH:14]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:27]([C:29]1([C:38]2[CH:43]=[CH:42][CH:41]=[C:40]([OH:44])[CH:39]=2)[CH2:35][CH2:34][CH2:33][CH2:32][N:31]([CH3:36])[C:30]1=[O:37])[CH3:28].C(Cl)Cl>CO>[C:1]([O:5][C:6](=[O:26])[NH:7][CH2:8][CH2:9][C:10]1[N:11]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[C:19]([O:44][C:40]3[CH:41]=[CH:42][CH:43]=[C:38]([C:29]4([CH2:27][CH3:28])[CH2:35][CH2:34][CH2:33][CH2:32][N:31]([CH3:36])[C:30]4=[O:37])[CH:39]=3)[CH:18]=2)[C:12]([CH3:15])=[N:13][CH:14]=1)([CH3:4])([CH3:3])[CH3:2].[NH4+:7].[OH-:5]

Participants

6

Reactant 3

HCID 6344DichloromethaneHCID 27945733-Ethylhexahydro-3-(3-hydroxyphenyl)-1-methyl-2H-azepin-2-oneHCID 70159417{2-[3-(4-cyano-3-fluoro-benzyl)-2-methyl-3H-imidazol-4-yl]-ethyl}-carbamic acid tert-butyl ester

Product 2

HCID 14923Ammonium HydroxideHCID 54508564[2-(3-{4-cyano-3-[3-(3-ethyl-1-methyl-2-oxo-azepan-3-yl)-phenoxy]-benzyl}-2-methyl-3H-imidazol-4-yl)-ethyl]-carbamic acid tert-butyl ester

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Following the procedure outlined in Example 2, but using {2-[3-(4-cyano-3-fluoro-benzyl)-2-methyl-3H-imidazol-4-yl]-ethyl}-carbamic acid tert-butyl ester (as described in Step A above) (0.60 g, 1.67 mmol) and 3-ethyl-3-(3-hydroxy-phenyl)-1-methyl-azepan-2-one (0.41 g, 1.67 mmol), the title compound was obtained after chromatography (CH2Cl2:CH3OH:NH4OH, 98:2:0.2).

Sources & evidence

ORD record
ord-d35ba693f19b448c9334bb724619cca8
Source dataset
uspto-grants-2001_09
Patent number
US06284755B1

Reaction notes

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