Propionyl chloride → HCID 21876366, compound

HRID 1454633Notes

Reaction equation

[NH2:1][C:2]1[CH:3]=[C:4]([S:18]([NH:21][C:22]([CH3:25])([CH3:24])[CH3:23])(=[O:20])=[O:19])[CH:5]=[CH:6][C:7]=1[NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][Cl:17])=[CH:11][CH:10]=1.[C:26](Cl)(=O)[CH2:27][CH3:28]>>[C:22]([NH:21][S:18]([C:4]1[CH:5]=[CH:6][C:7]2[N:8]([C:9]3[CH:10]=[CH:11][C:12]([CH2:15][CH2:16][Cl:17])=[CH:13][CH:14]=3)[C:26]([CH2:27][CH3:28])=[N:1][C:2]=2[CH:3]=1)(=[O:19])=[O:20])([CH3:25])([CH3:24])[CH3:23]

Participants

Reactant 2

HCID 62324Propionyl chloride

HCID 21876208HCID 21876208, compound

Product 1

HCID 21876366HCID 21876366, compound

Procedure

The title compound was prepared according to the procedure described in step 5 Example 1 from 3-amino-N-(tert-butyl)-4-[4-(2-chloroethyl)anilino]benzenesulfonamide (step 4) and propionyl chloride.

Sources & evidence

ORD record: ord-b3650943eb494245b53f0a6d960321b4
Source dataset: uspto-grants-2009_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07479564B2

Reaction notes

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