N-Hydroxysuccinimide → HCID 86655526, compound
Reaction equation
[C:1]([C:3](=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[F:14])[C:4]([OH:6])=[O:5])#[N:2].O[N:16]1[C:20](=[O:21])[CH2:19][CH2:18][C:17]1=[O:22].CCN=C=NCCCN(C)C.Cl>C(Cl)Cl>[C:1]([C:3](=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[F:14])[C:4]([O:6][N:16]1[C:20](=[O:21])[CH2:19][CH2:18][C:17]1=[O:22])=[O:5])#[N:2]Participants
5
Procedure
The same procedures as in Example 119 were carried out from α-cyano-2-fluorocinnamic acid (12.0 g), N-hydroxysuccinic acid imide (10.8 g), WSC.HCl (18.1 g), and methylene chloride (300 mL), to give the captioned compound (8.0 g, 44%) as crystals.
Sources & evidence
- ORD record
- ord-2ad8a245bd6949488d3d61fd2e8255f5
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09150510B2
Reaction notes
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