Putrescine → 4-Amino-N-[S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteinyl]butylamine

HRID 249574Notes

Reaction equation

[CH2:1]([S:8][CH2:9][C@@H:10]([C:26]([OH:28])=O)[NH:11][C:12](=[O:25])[C:13]([CH3:24])([CH3:23])[CH2:14][S:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:29][CH2:30][CH2:31][CH2:32][CH2:33][NH2:34]>>[NH2:29][CH:30]([C:26](=[O:28])[C@H:10]([CH2:9][S:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[NH:11][C:12](=[O:25])[C:13]([CH3:23])([CH3:24])[CH2:14][S:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1)[CH2:31][CH2:32][CH2:33][NH2:34]

Participants

Reactant 2

HCID 1045Putrescine

HCID 14969990S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteine

Product 1

HCID 677875534-Amino-N-[S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteinyl]butylamine

Procedure

S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteine and 1,4-diaminobutane were used as starting materials.

Sources & evidence

ORD record: ord-bdd88793098b4bb3814795a5e3b0da6b
Source dataset: uspto-grants-1993_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05214181

Reaction notes

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