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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329863Generated: October 30, 2026

2,3-Dichlorobenzaldehyde → HCID 19871227, compound

https://huagongshe.com/reaction/329863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichlorobenzaldehydeHCID 35745—
Reactant2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
ReactantHCID 19871204HCID 19871204—
SolventIsopropanolHCID 3776—
ProductHCID 19871227HCID 1987122727.3%

Reaction Steps

A mixture of 2,3-dichlorobenzaldehyde, 2-[4-(4,4'-dimethylbenzhydryl)-1-piperazinyl]ethyl acetoacetate and ethyl 3-aminocrotonate was worked up in isopropyl alcohol in the same manner as Example 1 to give 2-[4-(4,4'-dimethylbenzhydryl)-1-piperazinyl]ethyl ethyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 85°-88° C. (sintering). Yield 27.3%. IR(Nujol)cm-1 : 3330, 1690. NMR(CDCl3) δ: 1.14(3H,t,J=7,--CH2CH3), 2.25(12H,s, ##STR37## 4.05(2H,q,J=7,--CH2CH3), 4.08(1H,s,>N--CH<), 4.08(2H,t, J=6,--COOCH2CH2 --), 5.41(1H,s,C(4) --H), 5.68(1H,broad s, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892875
Source datasetuspto-grants-1990_01
ORD IDord-0a5715abcc0644c6b124525d80488494
Source noteuspto-grants-1990_01