4-Nitro-2-phenylbenzoic acid → [4-(3-Pyridylmethyloxy)-2-phenylbenzoyl]methionine methyl ester

HRID 2121209Notes

Reaction equation

HRID 2121209 reaction equation
Cl.[CH3:2][O:3][C:4](=[O:26])[C@H:5]([CH2:22][CH2:23][S:24][CH3:25])[NH:6][C:7](=[O:21])[C:8]1[CH:13]=[CH:12][C:11](N)=[CH:10][C:9]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[N:27]1[CH:32]=[CH:31][CH:30]=[C:29]([CH2:33][O:34]C2C=CC(C(O)=O)=C(C3C=CC=CC=3)C=2)[CH:28]=1.[N+](C1C=CC(C(O)=O)=C(C2C=CC=CC=2)C=1)([O-])=O>>[CH3:2][O:3][C:4](=[O:26])[C@H:5]([CH2:22][CH2:23][S:24][CH3:25])[NH:6][C:7](=[O:21])[C:8]1[CH:13]=[CH:12][C:11]([O:34][CH2:33][C:29]2[CH:28]=[N:27][CH:32]=[CH:31][CH:30]=2)=[CH:10][C:9]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

4

Reactant 3

HCID 106578414-Nitro-2-phenylbenzoic acidHCID 234360264-(3-Pyridylmethyloxy)-2-phenylbenzoic acidHCID 69612387(4-Amino-2-phenylbenzoyl)methionine methyl ester hydrochloride

Product 1

HCID 53751775[4-(3-Pyridylmethyloxy)-2-phenylbenzoyl]methionine methyl ester

Procedure

The desired compound was prepared by according to the procedure used in step C of the preparation of compound 8, except substituting 4-(3-pyridylmethyloxy)-2-phenylbenzoic acid, prepared as in Example 240E, for 4-nitro-2-phenylbenzoic acid.

Sources & evidence

ORD record
ord-a21d65c3ed6a4ce2aad7f30bd008b9ec
Source dataset
uspto-grants-2004_02
Patent number
US06693123B2

Reaction notes

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