4-Cyanobenzaldehyde → HCID 19871205, compound

HRID 329875Notes

Reaction equation

HRID 329875 reaction equation
[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1)#[N:2].[C:11]([O:17][CH2:18][CH2:19][N:20]1[CH2:25][CH2:24][N:23]([CH:26]([C:34]2[CH:39]=[CH:38][C:37]([CH3:40])=[CH:36][CH:35]=2)[C:27]2[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=2)[CH2:22][CH2:21]1)(=[O:16])[CH2:12][C:13]([CH3:15])=O.[NH2:41]/[C:42](/[CH3:49])=[CH:43]\[C:44]([O:46][CH2:47][CH3:48])=[O:45]>C(O)(C)C>[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]2[C:43]([C:44]([O:46][CH2:47][CH3:48])=[O:45])=[C:42]([CH3:49])[NH:41][C:13]([CH3:15])=[C:12]2[C:11]([O:17][CH2:18][CH2:19][N:20]2[CH2:25][CH2:24][N:23]([CH:26]([C:27]3[CH:28]=[CH:29][C:30]([CH3:33])=[CH:31][CH:32]=3)[C:34]3[CH:35]=[CH:36][C:37]([CH3:40])=[CH:38][CH:39]=3)[CH2:22][CH2:21]2)=[O:16])=[CH:5][CH:4]=1)#[N:2]

Participants

5

Reactant 3

HCID 660424-CyanobenzaldehydeHCID 6437562-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 19871204HCID 19871204, compound

Product 1

HCID 19871205HCID 19871205, compound

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

A mixture of p-cyanobenzaldehyde, 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-(4-cyanophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 93°-96° C. (sintering). Yield 61.9. IR(Nujol)cm-1 : 3330, 2220, 1685. NMR(CDCl3) δ: 1.15(3H,t,J=7,--CH2CH3), 2.24(6H,s, ##STR51## 2.29(6H,s, ##STR52## 4.03(2H,q,J=7,--CH2CH3), 4.11(1H,s,>N--CH<), 4.13(2H,t,J=7,--COOCH2 --), 5.01(1H, s,C(4) --H), 5.77(1H,broad s, NH).

Sources & evidence

ORD record
ord-cb371496b70741e4a12a826730df8002
Source dataset
uspto-grants-1990_01
Patent number
US04892875

Reaction notes

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