HCID 53719967, compound → HCID 69780937, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C@@H:8]([O:35][Si](C(C)(C)C)(C)C)[CH2:9][N:10](C(OC(C)(C)C)=O)[CH2:11][CH2:12][NH:13][C:14]2[CH:15]=[C:16]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([C:26]#[N:27])[CH:21]=3)[CH:17]=[CH:18][CH:19]=2)[CH:5]=[CH:6][CH:7]=1>Cl.O1CCOCC1>[ClH:1].[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([C@@H:8]([OH:35])[CH2:9][NH:10][CH2:11][CH2:12][NH:13][C:14]2[CH:15]=[C:16]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([C:26]#[N:27])[CH:21]=3)[CH:17]=[CH:18][CH:19]=2)[CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
m.p. 191-206° C.; from (R)-3′-[[2-[[2-(3-chlorophenyl)-2-[[(tert-butyl)dimethylsilyl]oxy]ethyl][(tert-butoxy)carbonyl]amino]ethyl]amino]-[1,1′-biphenyl]-3-carbonitrile (173 mg) in 4 N hydrochloric acid in dioxane (10 mL).
Sources & evidence
- ORD record
- ord-ec4755a4e0474466b5585ca30dd8fa28
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06251925B1
Reaction notes
Loading…