2-Chloro-5-nitropyridine → HCID 86690161, compound

HRID 1500212Notes

Reaction equation

HRID 1500212 reaction equation
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[CH:11]([C:13]1[C:14]([O:23][CH2:24][CH2:25][CH2:26][CH3:27])=[C:15](B(O)O)[CH:16]=[C:17]([CH3:19])[CH:18]=1)=[O:12]>>[CH2:24]([O:23][C:14]1[C:15]([C:2]2[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=2)=[CH:16][C:17]([CH3:19])=[CH:18][C:13]=1[CH:11]=[O:12])[CH2:25][CH2:26][CH3:27]

Participants

3

Reactant 2

HCID 783082-Chloro-5-nitropyridineHCID 16217233(2-Butoxy-3-formyl-5-methylphenyl)boronic acid

Product 1

HCID 86690161HCID 86690161, compound

Procedure

The title compound was synthesized in a manner analogous to Example 52(i), except for replacing 2-chloro-5-nitropyridin with 2-chloro-5-nitropyridine, and replacing 3-formyl-2-isopropoxy-5-methylphenylboronic acid with 3-formyl-2-butoxy-5-methylphenylboronic acid.

Sources & evidence

ORD record
ord-45cd9a4132ef47f0a2a01ab376bbf344
Source dataset
uspto-grants-2015_12
Patent number
US09206129B2

Reaction notes

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