HCID 44818005, compound → HCID 67221700, compound

HRID 390064Notes

Reaction equation

HRID 390064 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][NH:5][C:6]1[N:7]=[C:8]([NH:17][C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[CH:19]=2)[C:9]2[C:15](=[O:16])[NH:14][CH:13]=[CH:12][C:10]=2[N:11]=1.NCCCN[C:30]([C@@H:32]1[CH2:36][S:35][C:34](=[O:37])[NH:33]1)=[O:31]>>[CH3:24][C:20]1[CH:19]=[C:18]([NH:17][C:8]2[C:9]3[C:15](=[O:16])[NH:14][CH:13]=[CH:12][C:10]=3[N:11]=[C:6]([NH:5][CH2:4][CH2:3][CH2:2][NH:1][C:30]([C@@H:32]3[CH2:36][S:35][C:34](=[O:37])[NH:33]3)=[O:31])[N:7]=2)[CH:23]=[CH:22][CH:21]=1

Participants

3

Reactant 2

HCID 44818005HCID 44818005, compoundHCID 67221680HCID 67221680, compound

Product 1

HCID 67221700HCID 67221700, compound

Procedure

The compound was prepared from 2-[(3-aminopropyl)amino]-4-[(3-methylphenyl)amino]pyrido[4,3-d]pyrimidin-5(6H)-one and (4R)—N-(3-aminopropyl)-2-oxo-1,3-thiazolidine-4-carboxamide using the procedure similar to that described for Example

Sources & evidence

ORD record
ord-d7a5ebbca7c741088662b3bc40d0783e
Source dataset
uspto-grants-2013_02
Patent number
US08383635B2

Reaction notes

Loading…