2-Chloroethylammonium chloride → 2-(4-Nitrophenylimino)-1,3-thiazolidine

Reaction equation

[Cl-].Cl[CH2:3][CH2:4][NH3+:5].[N+:6]([C:9]1[CH:14]=[CH:13][C:12]([N:15]=[C:16]=[S:17])=[CH:11][CH:10]=1)([O-:8])=[O:7]>>[N+:6]([C:9]1[CH:10]=[CH:11][C:12]([N:15]=[C:16]2[NH:5][CH2:4][CH2:3][S:17]2)=[CH:13][CH:14]=1)([O-:8])=[O:7]

Participants

Reactant 2

HCID 133682-Chloroethylammonium chloride

HCID 75044Benzene, 1-isothiocyanato-4-nitro-

Product 1

HCID 1785266832-(4-Nitrophenylimino)-1,3-thiazolidine

Procedure

2-Chloroethylammonium chloride (Entry 1) was reacted with 4-nitrophenyl isothiocyanate according to Method C1a to give 2-(4-nitrophenylimino) -1,3-thiazolidine, which was reacted with isobutyl bromide according to Method D2a to give 2-(4-nitrophenylimino)-3-isobutyl-1,3-thiazolidine.

Sources & evidence

ORD record: ord-9c2c3adbfc094af49dee06f5e44b302e
Source dataset: uspto-grants-2002_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06353006B1

Reaction notes

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