Diethylamine → HCID 178446035, compound
Reaction equation
C(NCC)C.[NH:6](C(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O)[C@@H:7]([C:12]([NH:14][C@H:15]([C:23]([NH:25][C@@H:26]([C:30]([O:32][CH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)=[O:31])[CH:27]([CH3:29])[CH3:28])=[O:24])[CH2:16][CH2:17][CH2:18][NH:19][C:20](=[NH:22])[NH2:21])=[O:13])[CH2:8][CH:9]([CH3:11])[CH3:10]>CN(C)C=O>[NH2:6][C@@H:7]([C:12]([NH:14][C@H:15]([C:23]([NH:25][C@@H:26]([C:30]([O:32][CH2:33][C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1)=[O:31])[CH:27]([CH3:29])[CH3:28])=[O:24])[CH2:16][CH2:17][CH2:18][NH:19][C:20](=[NH:21])[NH2:22])=[O:13])[CH2:8][CH:9]([CH3:10])[CH3:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
12.05 ml of diethylamine are added to a solution of 8.04 g (11.5 mmol) of Fmoc-D-Leu-Arg-D-Val-OBzl in 60 ml of dimethylformamide. The mixture is left to stand at room temperature for 15 minutes, and is concentrated. The residue is partitioned between n-pentanol and NaHCO3 solution. The pentanol phase is concentrated, and the residue is triturated with diethyl ether.
Workup
- waitThe mixture is left
- concentrationis concentrated
- customThe residue is partitioned between n-pentanol and NaHCO3 solution
- concentrationThe pentanol phase is concentrated
- customthe residue is triturated with diethyl ether
Sources & evidence
- ORD record
- ord-24a30bd4d6934c87b1cf7d6f453e1400
- Source dataset
- uspto-grants-1991_04
- Patent number
- US05011825
Reaction notes
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