3-(4-Aminophenyl)prop-2-enoic acid → HCID 178479370, compound

HRID 1282714Notes

Reaction equation

HRID 1282714 reaction equation
[NH2:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7][C:8](O)=[O:9])=[CH:4][CH:3]=1.[ClH:13].[NH:14](C1C=C(C=CC=1)C([Cl:23])=O)[C:15](N)=[NH:16]>>[ClH:23].[NH:1]([C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7][C:8]([Cl:13])=[O:9])=[CH:4][CH:3]=1)[C:15]([NH2:16])=[NH:14]

Participants

3

Reactant 2

HCID 929283-(4-Aminophenyl)prop-2-enoic acidHCID 178479371HCID 178479371, compound

Product 1

HCID 178479370HCID 178479370, compound

Procedure

The 4-guanidinocinnamoyl chloride hydrochloride was prepared from 4-aminocinnamic acid according to the procedure of Example XII for preparing 3-guanidinobenzoyl chloride hydrochloride.

Sources & evidence

ORD record
ord-c08af1660f554eaab51949ce0e9f2603
Source dataset
uspto-grants-1976_08
Patent number
US03972872

Reaction notes

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