N,N-Diethyl-p-phenylenediamine → HCID 63545725, compound

HRID 1593518Notes

Reaction equation

HRID 1593518 reaction equation
Cl[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[CH2:11]([N:13]([CH2:21][CH3:22])[C:14]1[CH:19]=[CH:18][C:17]([NH2:20])=[CH:16][CH:15]=1)[CH3:12]>>[S:3]1[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=[C:2]1[NH:20][C:17]1[CH:16]=[CH:15][C:14]([N:13]([CH2:21][CH3:22])[CH2:11][CH3:12])=[CH:19][CH:18]=1

Participants

3

Reactant 2

HCID 7120N,N-Diethyl-p-phenylenediamineHCID 119872-Chlorobenzothiazole

Product 1

HCID 63545725HCID 63545725, compound

Procedure

The title compound was synthesised from 2-Chloro-benzothiazole (commercially available) and N,N-Diethyl-p-phenylenediamine (commercially available) according to the procedure described for Example 1a) above. MS (m/e): 298.2 (MH+, 100%).

Sources & evidence

ORD record
ord-889773eef7594aa5a4b1b127d3e45c43
Source dataset
uspto-grants-2007_11
Patent number
US07297707B2

Reaction notes

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