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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016108Generated: October 26, 2026

3-Chlorobenzoic Acid → 4-Chloro-N-(1-(4-(4-chlorophenyl)-5,6-dihydropyridin-1(2H)-yl)-1-oxobutan-2-yl)benzamide

https://huagongshe.com/reaction/1016108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzoic AcidHCID 447—
Reactant4-Chlorobenzoic AcidHCID 6318—
Reactant4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
ReactantAlanine, ethyl ester, hydrochloride (1:1)HCID 102560—
Reactant4-(4-chlorophenyl)piperidine HydrochlorideHCID 2757843—
ReactantMethyl 2-aminobutanoate hydrochlorideHCID 13283515—
Product4-Chloro-N-(1-(4-(4-chlorophenyl)-5,6-dihydropyridin-1(2H)-yl)-1-oxobutan-2-yl)benzamideHCID 57889233—

Reaction Steps

Example 224 was prepared in a similar manner as described for the preparation of Example 221 with the exceptions that 2-aminobutyric acid methyl ester hydrochloride was substituted for DL-alanine ethyl ester hydrochloride in Step 1, 4-chlorobenzoic acid was substituted for 3-chlorobenzoic acid in Step 2, and 4-(4-chlorophenyl)-4-hydroxypiperidine was substituted for 4-(4-chlorophenyl)piperidine hydrochloride in Step 4. Example 224 was provided by elimination during Step 5. MS found: (M+H)+=417.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-19f39b401a124bf58b4cd77cf344b526
Source noteuspto-grants-2011_07