HCID 54210211, compound → HCID 70076284, compound

HRID 344506Notes

Reaction equation

HRID 344506 reaction equation
Cl.Cl.[NH2:3][C:4]1[C:19]([Cl:20])=[CH:18][C:7]([C:8]([NH:10][CH2:11][CH:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)=[O:9])=[C:6]([O:21][CH3:22])[CH:5]=1.[CH:23]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH:26]=[CH:25][C:24]=1[CH2:33][O:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39]Cl>>[ClH:20].[NH2:3][C:4]1[C:19]([Cl:20])=[CH:18][C:7]([C:8]([NH:10][CH2:11][CH:12]2[CH2:13][CH2:14][N:15]([CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][O:34][CH2:33][C:24]3[CH:25]=[CH:26][C:27]4[C:32](=[CH:31][CH:30]=[CH:29][CH:28]=4)[CH:23]=3)[CH2:16][CH2:17]2)=[O:9])=[C:6]([O:21][CH3:22])[CH:5]=1

Participants

3

Reactant 2

HCID 54210211HCID 54210211, compoundHCID 699663304-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide dihydrochloride

Product 1

HCID 70076284HCID 70076284, compoundYield 95.9%

Procedure

4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide dihydrochloride (2.00 g) as starting compound and 5-(2-naphthylmethoxy)-pentyl chloride (1.88 g) were reacted and treated in the same manner as in Example 168 to give 1.45 g of 4-amino-5-chloro-2-methoxy-N-((1-(5-(2-naphthylmethoxy)pentyl)piperidin-4-yl)methyl)benzamide hydrochloride.

Workup

  1. customwere reacted
  2. additiontreated in the same manner as in Example 168

Sources & evidence

ORD record
ord-4349e6936aef4419bada634c4f634fae
Source dataset
uspto-grants-1999_01
Patent number
US05864039

Reaction notes

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