Carbodiimide → HCID 131716084, compound
Reaction equation
[NH:1]([C:14]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:15])[C@H:2]([C:11]([OH:13])=O)[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.Cl.C(O[C:32](=[O:43])[C@H:33]([CH2:35][C:36]1[CH:41]=[CH:40][C:39]([OH:42])=[CH:38][CH:37]=1)[NH2:34])CCCCC.N=C=N>>[NH:1]([C:14]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:15])[C@H:2]([C:11]([NH:34][C@H:33]([C:32]([CH2:11][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])=[O:43])[CH2:35][C:36]1[CH:37]=[CH:38][C:39]([OH:42])=[CH:40][CH:41]=1)=[O:13])[CH2:3][C:4]1[CH:5]=[CH:6][C:7]([OH:10])=[CH:8][CH:9]=1Participants
4
Procedure
Z-Tyr-Tyr-Hex was prepared from Z-Tyr and Tyr-Hex.HCl by the carbodiimide coupling technique. Yield of crude product: 89%.
Sources & evidence
- ORD record
- ord-356dda8180c24e72a87d1860463c69be
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04863735
Reaction notes
Loading…