Hydrochloric Acid → HCID 14182249, compound

HRID 1252703Notes

Reaction equation

HRID 1252703 reaction equation
[CH2:1]([N:3]1[CH2:8][CH2:7][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[C:5]([C:15]([N:17]([CH:21]([CH3:23])[CH3:22])[CH:18]([CH3:20])[CH3:19])=[O:16])[CH2:4]1)[CH3:2].[ClH:24]>>[ClH:24].[CH2:1]([N:3]1[CH2:8][CH2:7][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[C:5]([C:15]([N:17]([CH:21]([CH3:22])[CH3:23])[CH:18]([CH3:20])[CH3:19])=[O:16])[CH2:4]1)[CH3:2]

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 14182248HCID 14182248, compound

Product 1

HCID 14182249HCID 14182249, compound

Procedure

Employing the general method of Example 8, 1-ethyl-1,2,5,6-tetrahydro-N,N-bis(1-methylethyl)-4-phenyl-3-pyridinecarboxamide was prepared as the monohydrochloride salt, mp 208°-210° C.

Sources & evidence

ORD record
ord-7d0fcbb6ada24ac187589de704d01260
Source dataset
uspto-grants-1988_05
Patent number
US04745123

Reaction notes

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