Succinyl chloride → N,N'-Bis-((R)-1-indanyl)succinamide
Reaction equation
[NH2:1][C@H:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3]1.[C:11](Cl)(=[O:17])[CH2:12][CH2:13][C:14](Cl)=[O:15]>>[C@H:2]1([NH:1][C:11](=[O:17])[CH2:12][CH2:13][C:14]([NH:1][C@H:2]2[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[CH2:4][CH2:3]2)=[O:15])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3]1Participants
3
Procedure
This was prepared by the same procedure as in Example 73 starting from (R)-1-aminoindan (8.02 g, 60 mmole) and succinoyl chloride (2.32 g, 14 mmole), to give the white product, (1.30 g, 26.7%). Melting point: 266-9° C.
Workup
- customto give the white product, (1.30 g, 26.7%)
Sources & evidence
- ORD record
- ord-2c030952cbd5487ca4cba3b6747a8bbf
- Source dataset
- uspto-grants-1999_06
- Patent number
- US05914349
Reaction notes
Loading…