2-Propoxybenzamide → n-Propoxybenzamidine methyl sulfate

HRID 437419

Reaction equation

[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([NH2:9])=O)[CH2:2][CH3:3].[CH3:14][O:15][S:16]([OH:19])(=[O:18])=[O:17].C(OC1C=CC=CC=1C(N)=[NH:26])C>>[CH3:14][O:15][S:16]([OH:19])(=[O:18])=[O:17].[CH2:1]([O:4][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([NH2:26])=[NH:9])[CH2:2][CH3:3]

Participants

Reactant 2

HCID 430512-Propoxybenzamide

HCID 867348682-Ethoxybenzamidine methyl sulfate

Product 1

HCID 86734867n-Propoxybenzamidine methyl sulfateYield 74%

Procedure

The title compound (74% yield) was prepared from 2-n-propoxybenzamide in a manner similar to that described for the preparation of 2-ethoxybenzamidine methyl sulfate in Preparation 6 above.

Sources & evidence

ORD record: ord-2a143fe6e4f24c9194af94123b43c5c1
Source dataset: uspto-grants-1977_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04031093

Linked notes

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