2-Methoxybenzaldehyde → (3-Amino-5-chloro-pyridin-2-yl)-(2-methoxy-phenyl)-methanone

HRID 1898053Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]=[O:6].[Cl:11][C:12]1[CH:13]=[C:14]([N+:19]([O-])=O)[C:15](I)=[N:16][CH:17]=1>>[NH2:19][C:14]1[C:15]([C:5]([C:4]2[CH:7]=[CH:8][CH:9]=[CH:10][C:3]=2[O:2][CH3:1])=[O:6])=[N:16][CH:17]=[C:12]([Cl:11])[CH:13]=1

Participants

Reactant 2

HCID 86582-Methoxybenzaldehyde

HCID 579421085-Chloro-2-iodo-3-nitropyridine

Product 1

HCID 57942227(3-Amino-5-chloro-pyridin-2-yl)-(2-methoxy-phenyl)-methanone

Procedure

(3-Amino-5-chloro-pyridin-2-yl)-(2-methoxy-phenyl)-methanone was prepared from 2-methoxybenzaldehyde and 5-chloro-2-iodo-3-nitro-pyridine in three steps according to the General Procedure C. MS m/z: 263.1 (M+H).

Sources & evidence

ORD record: ord-eed1dfc5be514c1d8397e3eda19b5287
Source dataset: uspto-grants-2013_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08519135B2

Reaction notes

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