2-Butynedioic acid → HCID 54073641, compound
Reaction equation
[CH2:1]([NH:7][C:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[S:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[C:17]([C:22](O)=[O:23])#[C:18][C:19]([OH:21])=[O:20]>>[CH2:1]([N:7]1[C:22](=[O:23])[C:17](=[CH:18][C:19]([OH:21])=[O:20])[S:9][C:8]1=[N:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]Participants
3
Procedure
Prepared by the method described in Example 1 from N-hexyl-N'-phenylthiourea (3.4 g, 14 mmoles) and acetylenedicarboxylic acid (1.7 g, 14 mmoles). Recrystallization from acetonitrile gave the product (3.0 g), mp 145°-146° C.
Workup
- customPrepared by the method
- customRecrystallization from acetonitrile
Sources & evidence
- ORD record
- ord-1860d8d8e6274290a658efd98d161659
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04775677
Reaction notes
Loading…