HCID 67021570, compound → HCID 67021599, compound

HRID 1010727Notes

Reaction equation

HRID 1010727 reaction equation
[CH3:1][O:2][C:3](=[O:22])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[C:17]([N+:18]([O-])=O)=[CH:16][CH:15]=[CH:14][N:13]=2)=[CH:7][C:6]=1[CH3:21]>[Ni]>[CH3:1][O:2][C:3](=[O:22])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[C:17]([NH2:18])=[CH:16][CH:15]=[CH:14][N:13]=2)=[CH:7][C:6]=1[CH3:21]

Participants

3

Procedure

A suspension of 2.2 g of [2-methyl-4-(3-nitro-pyridin-2-ylamino)-phenyl]-acetic acid methyl ester and 220 mg of Raney Ni is stirred for 6.5 hours at rt under a hydrogen atmosphere. The mixture obtained is filtered through a pad of celite and concentrated. [4-(3-Amino-pyridin-2-ylamino)-2-methyl-phenyl]-acetic acid methyl ester is obtained. ES-MS: 272.1 [M+H]+; tR=2.53 min (System 1).

Workup

  1. customThe mixture obtained
  2. filtrationis filtered through a pad of celite and
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-9bdee7ab9ca7446dbdb8f23febb47f91
Source dataset
uspto-grants-2011_07
Patent number
US07977338B2

Reaction notes

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