HCID 21440124, compound → HCID 21440198, compound

HRID 328945Notes

Reaction equation

HRID 328945 reaction equation
C(C1C([N+]([O-])=O)=CC(C(O)=O)=CC=1OCCCC)(=O)C1C=CC=CC=1.[C:26]([C:34]1[C:42]([N+:43]([O-])=O)=[CH:41][C:37]([C:38]([OH:40])=[O:39])=[CH:36][C:35]=1[O:46][CH2:47][C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][N:49]=1)(=[O:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[NH2:43][C:42]1[C:34]([C:26](=[O:33])[C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[C:35]([O:46][CH2:47][C:48]2[CH:53]=[CH:52][CH:51]=[CH:50][N:49]=2)[CH:36]=[C:37]([CH:41]=1)[C:38]([OH:40])=[O:39]

Participants

3

Reactant 2

HCID 21440124HCID 21440124, compoundHCID 21440130HCID 21440130, compound

Product 1

HCID 21440198HCID 21440198, compound

Procedure

By replacing in Example 1, step C, 4-benzoyl-3-n-butoxy-5-nitrobenzoic acid with 4-benzoyl-5-nitro-3-(2-pyridylmethoxy)benzoic acid, and following the procedure described, 5-amino-4-benzoyl-3-(2-pyridylmethoxy)benzoic acid is obtained with a melting point of 212°-213° C.

Sources & evidence

ORD record
ord-3e1453efc5fc4a4e8ee0117e6f3d6419
Source dataset
uspto-grants-1977_04
Patent number
US04018794

Reaction notes

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