4-Amino-5-chloro-2-(2-propenyloxy)benzoic acid → 4-Amino-N-(1-azabicyclo[3.2.1]oct-5-ylmethyl)-5-chloro-2-(2-propenyloxy)benzamide

HRID 5388Notes

Reaction equation

HRID 5388 reaction equation
[NH2:1][C:2]1[C:10]([Cl:11])=[CH:9][C:5]([C:6]([OH:8])=O)=[C:4]([O:12][CH2:13][CH:14]=[CH2:15])[CH:3]=1.[N:16]12[CH2:23][C:20]([CH2:24][NH2:25])([CH2:21][CH2:22]1)[CH2:19][CH2:18][CH2:17]2>>[NH2:1][C:2]1[C:10]([Cl:11])=[CH:9][C:5]([C:6]([NH:25][CH2:24][C:20]23[CH2:23][N:16]([CH2:22][CH2:21]2)[CH2:17][CH2:18][CH2:19]3)=[O:8])=[C:4]([O:12][CH2:13][CH:14]=[CH2:15])[CH:3]=1

Participants

3

Reactant 2

HCID 117463644-Amino-5-chloro-2-(2-propenyloxy)benzoic acidHCID 19795979{1-Azabicyclo[3.2.1]octan-5-yl}methanamine

Product 1

HCID 197959954-Amino-N-(1-azabicyclo[3.2.1]oct-5-ylmethyl)-5-chloro-2-(2-propenyloxy)benzamide

Procedure

Following the procedure of Example 1, the title compound is prepared from 4-amino-5-chloro-2-(2-propenyloxy)benzoic acid and 1-azabicyclo[3.2.1]octan-5-methanamine.

Sources & evidence

ORD record
ord-1339d8a661144dc8b56716544887dca6
Source dataset
uspto-grants-1993_09
Patent number
US05244907

Reaction notes

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