Propionyl chloride → HCID 86611498, compound

HRID 724102Notes

Reaction equation

[NH2:1][C:2]1[CH:20]=[C:19]([Cl:21])[C:18]([Cl:22])=[CH:17][C:3]=1[NH:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:7][CH:6]=1.[C:23](Cl)(=O)[CH2:24][CH3:25]>>[Cl:21][C:19]1[C:18]([Cl:22])=[CH:17][C:3]2[N:4]([C:5]3[CH:10]=[CH:9][C:8]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:7][CH:6]=3)[C:23]([CH2:24][CH3:25])=[N:1][C:2]=2[CH:20]=1

Participants

Reactant 2

HCID 62324Propionyl chloride

HCID 86611499HCID 86611499, compound

Product 1

HCID 86611498HCID 86611498, compound

Procedure

The title compound was prepared according to the procedure described in step 5 of Example 1 from ethyl [4-(2-amino-4,5-dichloroanilino)phenyl]acetate (step 2) and propionyl chloride.

Sources & evidence

ORD record: ord-3104c02a648d47b4a7acc5392d91e8e8
Source dataset: uspto-grants-2006_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07141580B2

Reaction notes

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