Piperazine → HCID 20150168, compound

HRID 2308660Notes

Reaction equation

HRID 2308660 reaction equation
Cl[C:2]1[N:3]=[C:4]([N:23]2[CH2:28][CH2:27][O:26][CH2:25][CH2:24]2)[C:5]2[N:11]=[CH:10][N:9]=[C:8]([S:12][CH2:13][C:14]3[CH:19]=[CH:18][C:17]4[O:20][CH2:21][O:22][C:16]=4[CH:15]=3)[C:6]=2[N:7]=1.[NH:29]1[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]1>>[CH2:21]1[O:20][C:17]2[CH:18]=[CH:19][C:14]([CH2:13][S:12][C:8]3[C:6]4[N:7]=[C:2]([N:29]5[CH2:34][CH2:33][NH:32][CH2:31][CH2:30]5)[N:3]=[C:4]([N:23]5[CH2:28][CH2:27][O:26][CH2:25][CH2:24]5)[C:5]=4[N:11]=[CH:10][N:9]=3)=[CH:15][C:16]=2[O:22]1

Participants

3

Reactant 2

HCID 4837PiperazineHCID 20150187HCID 20150187, compound

Product 1

HCID 20150168HCID 20150168, compound

Procedure

This compound was prepared analogous to Example 1 from 2-chloro-8-(3,4-methylenedioxybenzyl-thio)-4-morpholino-pyrimido-[5,4-d]-pyrimidine (m.p.: 200°-202° C.) and piperazine.

Sources & evidence

ORD record
ord-801f0e792bdf480c98cc7a6d1e202448
Source dataset
uspto-grants-1987_09
Patent number
US04690923

Reaction notes

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