Dimethyl[2-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)ethyl]amine → HCID 22142969, compound

HRID 2297293Notes

Reaction equation

HRID 2297293 reaction equation
CN(C)CCNCCNC1C=CC([N+]([O-])=O)=CN=1.[N:19]1([CH2:25][CH2:26][N:27]([CH2:40][CH2:41][NH:42][C:43]2[CH:48]=[CH:47][C:46]([N+:49]([O-:51])=[O:50])=[CH:45][N:44]=2)S(C2C=CC=CC=2[N+]([O-])=O)(=O)=O)[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1>>[N:19]1([CH2:25][CH2:26][NH:27][CH2:40][CH2:41][NH:42][C:43]2[CH:48]=[CH:47][C:46]([N+:49]([O-:51])=[O:50])=[CH:45][N:44]=2)[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1

Participants

3

Reactant 2

HCID 22142526Dimethyl[2-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)ethyl]amineHCID 22142773HCID 22142773, compound

Product 1

HCID 22142969HCID 22142969, compound

Procedure

Made using the same procedure as for polymer-bound dimethyl[2-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)ethyl]amine except that resin-bound (2-morpholin-4-ylethyl){2-[(5-nitro(2-pyridyl))amino]ethyl}[(2-nitrophenyl)sulfonyl]amine was used.

Sources & evidence

ORD record
ord-0d5497358ef94aa984d25e02052ffe99
Source dataset
uspto-grants-2002_12
Patent number
US06489344B1

Reaction notes

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