Benzyl piperazine-1-carboxylate → HCID 57869401, compound
Reaction equation
[N:1]1([C:7](OCC2C=CC=CC=2)=O)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[N:17]1([C:24]2[CH:29]=[C:28](Cl)[N:27]=[C:26]([NH:31][C@H:32]3[CH2:36][CH2:35][N:34]([C:37](OC(C)(C)C)=O)[C@@H:33]3[CH2:44][CH2:45]C=O)[N:25]=2)[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1>>[N:17]1([C:24]2[CH:29]=[CH:28][N:27]=[C:26]([NH:31][C@H:32]3[CH2:36][CH2:35][N:34]([CH:37]4[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]4)[C@@H:33]3[CH2:44][CH2:45][CH2:7][N:1]3[CH2:2][CH2:3][NH:4][CH2:5][CH2:6]3)[N:25]=2)[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]1Participants
3
Procedure
The same procedure as a series of reactions of Example 21→Example 16→Example 21→Example 20 was carried out, except that benzyl piperazine-1-carboxylate was used in place of the compound 20 and the compound 40 was used in place of cyclohexanone in the process of Example 21, to obtain the title compound (1.13 g) having the following physical properties.
Sources & evidence
- ORD record
- ord-e3a4f0ee73a54956a4e4f3347832cc50
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08680092B2
Reaction notes
Loading…