HCID 23296428, compound → HCID 23296419, compound

HRID 1954395Notes

Reaction equation

HRID 1954395 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([N:12]2[CH2:21][CH2:20][C:19]3[C:14](=[CH:15][C:16]([N+:22]([O-])=O)=[CH:17][CH:18]=3)[CH2:13]2)=[O:11])=[CH:5][CH:4]=1)#[N:2]>[H][H].[Pd]>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH2:9][C:10]([N:12]2[CH2:21][CH2:20][C:19]3[C:14](=[CH:15][C:16]([NH2:22])=[CH:17][CH:18]=3)[CH2:13]2)=[O:11])=[CH:7][CH:8]=1)#[N:2]

Participants

3

Reactant 1

HCID 23296428HCID 23296428, compound

Product 1

HCID 23296419HCID 23296419, compound

Reagents, catalysts & solvents 1

HCID 178506449HCID 178506449, compoundCatalyst

Procedure

Prepared analogously to Example 1b from 2-[(4-cyanophenyl)-acetyl]-7-nitro-1,2,3,4-tetrahydro-isoquinoline and hydrogen/palladium.

Sources & evidence

ORD record
ord-382f532560094ba2bed7bba932392809
Source dataset
uspto-grants-2000_09
Patent number
US06121308

Reaction notes

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