Succinic anhydride → HCID 178525518, compound
Reaction equation
O([C@H]1CC[C@H](C[NH:12][C:13](=[O:19])[CH2:14][CH2:15][C:16]([OH:18])=[O:17])CC1)[N+]([O-])=O.[O:20]([C@H:24]1[CH2:29][CH2:28][C@H:27](CN)[CH2:26][CH2:25]1)[N+:21]([O-:23])=[O:22].C1(=O)OC(=O)CC1>>[O:20]([C@H:24]1[CH2:25][CH2:26][C@H:27]([NH:12][C:13](=[O:19])[CH2:14][CH2:15][C:16]([OH:18])=[O:17])[CH2:28][CH2:29]1)[N+:21]([O-:23])=[O:22]Participants
4
Procedure
N-(trans-4-nitroxycyclohexylmethyl)-succinic acid monoamide from trans-4-nitroxycyclohexylmethylamine and succinic acid anhydride melting point: 79°-81° C. (ether), yield: 80%.
Sources & evidence
- ORD record
- ord-6ee26559b0af496a8322303a209d5459
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05411989
Reaction notes
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