Piperazine → HCID 12817082, compound
Reaction equation
Cl[C:2]1[N:3]=[C:4]([N:16]2[CH2:21][CH2:20][S:19](=[O:22])[CH2:18][CH2:17]2)[C:5]2[N:11]=[CH:10][N:9]=[C:8]([NH:12][CH2:13][CH2:14][OH:15])[C:6]=2[N:7]=1.[NH:23]1[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]1>>[OH:15][CH2:14][CH2:13][NH:12][C:8]1[C:6]2[N:7]=[C:2]([N:23]3[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]3)[N:3]=[C:4]([N:16]3[CH2:21][CH2:20][S:19](=[O:22])[CH2:18][CH2:17]3)[C:5]=2[N:11]=[CH:10][N:9]=1Participants
3
Procedure
This compound was prepared analogous to Example 118 from 2-chloro-8-(2-hydroxyethyl-amino)-4-(1-oxido-thiomorpholino)-pyrimido-[5,4-d]-pyrimidine (m.p.: 227°-229° C.) and piperazine.
Sources & evidence
- ORD record
- ord-fdc6a8881e4342f396dfe29bd0a5de58
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04690923
Reaction notes
Loading…