4-Ethyl-2,3-dioxopiperazinecarbonyl chloride → HCID 20190187, compound
Reaction equation
Cl.[NH2:2][CH:3]([C:7]1[N:8]=[N:9][S:10][CH:11]=1)[C:4]([OH:6])=[O:5].[CH2:12]([N:14]1[CH2:19][CH2:18][N:17]([C:20](Cl)=[O:21])[C:16](=[O:23])[C:15]1=[O:24])[CH3:13]>>[CH2:12]([N:14]1[CH2:19][CH2:18][N:17]([C:20]([NH:2][CH:3]([C:7]2[N:8]=[N:9][S:10][CH:11]=2)[C:4]([OH:6])=[O:5])=[O:21])[C:16](=[O:23])[C:15]1=[O:24])[CH3:13]Participants
3
Procedure
The title compound (1.24 g) was prepared from 2-amino-2-(1,2,3-thiadiazol-4-yl)acetic acid hydrochloride [Example 3(a)] (912 mg) and 4-ethyl-2,3-dioxopiperazin-1-ylcarbonyl chloride (953 mg) by the method of Example 1(a).
Sources & evidence
- ORD record
- ord-7117754e6e8640b49cc4ad4fb2f2ff13
- Source dataset
- uspto-grants-1987_08
- Patent number
- US04684642
Reaction notes
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