Reaction equation
[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:20])[C:7]=1[S:8][C:9]1[S:13][C:12]([C:14]([OH:16])=O)=[CH:11][C:10]=1[N+:17]([O-:19])=[O:18].[OH:21][CH2:22][CH2:23][NH2:24]>>[Cl:20][C:6]1[CH:5]=[N:4][CH:3]=[C:2]([Cl:1])[C:7]=1[S:8][C:9]1[S:13][C:12]([C:14]([NH:24][CH2:23][CH2:22][OH:21])=[O:16])=[CH:11][C:10]=1[N+:17]([O-:19])=[O:18]Participants
3
Procedure
Prepared according to the procedure described for example 44 from 5-[(3,5-dichloro-4-pyridyl)sulfanyl]-4-nitro-thiophene-2-carboxylic acid (35 mg, 0.1 mmol) and 2-hydroxylethylamine (17.6 mg, 0.12 mmol). The title compound was obtained as a solid (7.8 mg, 17.0% yield). MS m/z: 347.80, 349.80 [M+H]+.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-04e64880a1fb465aa29df28e1f5fbbb7
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08680139B2
Linked notes
Loading…