HCID 68459528, compound → HCID 68464491, compound

HRID 503660Notes

Reaction equation

HRID 503660 reaction equation
[CH2:1]([O:8][C:9]1[CH:18]=[C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:16]=[C:15](Cl)[C:10]=1[C:11]([NH:13][NH2:14])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:28](OC1C=CC(C(NN)=O)=C(CC)C=1Cl)[C:29]1C=CC=CC=1>>[CH2:1]([O:8][C:9]1[CH:18]=[C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:16]=[C:15]([CH2:28][CH3:29])[C:10]=1[C:11]([NH:13][NH2:14])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 68459528HCID 68459528, compoundHCID 68461372HCID 68461372, compound

Product 1

HCID 68464491HCID 68464491, compound

Procedure

An analogous preparation procedure also gives 2,4-dibenzyloxy-6-chlorobenzohydrazide: yield 61%, m.p. 166-1670, and 4-benzyloxy-3-chloro-2-ethylbenzohydrazide: yield 85%, m.p. 182-1840.

Sources & evidence

ORD record
ord-a20087ab5e3145a5bb70b988df67ffad
Source dataset
uspto-grants-2010_08
Patent number
US07776920B2

Reaction notes

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