1,3-Propanediol → 4-t-butyl-N-[6-(3-hydroxypropyloxy)-2-(4-isopropylpiperazinyl)-5-(2-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamide
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH:14][C:15]2[C:20]([O:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[O:28][CH3:29])=[C:19](Cl)[N:18]=[C:17]([N:31]3[CH2:36][CH2:35][N:34]([CH:37]([CH3:39])[CH3:38])[CH2:33][CH2:32]3)[N:16]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:40]([OH:44])[CH2:41][CH2:42][OH:43]>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH:14][C:15]2[C:20]([O:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[O:28][CH3:29])=[C:19]([O:43][CH2:42][CH2:41][CH2:40][OH:44])[N:18]=[C:17]([N:31]3[CH2:36][CH2:35][N:34]([CH:37]([CH3:39])[CH3:38])[CH2:33][CH2:32]3)[N:16]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The procedure described in Synthesis Example 3 was repeated by use of 4-t-butyl-N-[6-chloro-2-(4-isopropyl -piperazinyl)-5-(2-methoxyphenoxy)-4-pyrimidinyl]-benzenesulfonamide and 1,3-propanediol, to thereby obtain the title compound as a pale yellow oil.
Workup
- customThe procedure described in Synthesis Example 3
Sources & evidence
- ORD record
- ord-94020c71235a41b48f3eb01b5cd17309
- Source dataset
- uspto-grants-1999_03
- Patent number
- US05883092
Reaction notes
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