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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329852Generated: October 30, 2026

2,3-Dichlorobenzaldehyde → HCID 19871210, compound

https://huagongshe.com/reaction/329852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichlorobenzaldehydeHCID 35745—
ReactantMethyl 3-aminocrotonateHCID 643918—
ReactantHCID 19871201HCID 19871201—
SolventIsopropanolHCID 3776—
ProductHCID 19871210HCID 1987121052.9%

Reaction Steps

A mixture of 2,3-dichlorobenzaldehyde, 2-[4-(4,4'-difluorobenzhydryl)-1-piperazinyl]ethyl acetoacetate and methyl 3-aminocrotonate was worked up in isopropyl alcohol in the same manner as Example 1 to give 2-[4-(4,4'-difluorobenzhydryl)-1-piperazinyl]ethyl methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 90°-93° C. (sintering). Yield 52.9%. IR(KBr)cm-1 : 3340, 1695. NMR(CDCl3) δ: 2.28(6H,s, ##STR24## 3.57(3H,s,COOCH3), 4.12(2H,t,J=6,--COOCH2CH2 --), 4.16(1H,s,>N--CH<), 5.42(1H,s,C(4) --H), 5.70(1H,broad s, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892875
Source datasetuspto-grants-1990_01
ORD IDord-f10eced2146d4fd2a05b61cd95be04cf
Source noteuspto-grants-1990_01