6-Chloroquinoline-4-carbaldehyde → 2-[(6-chloroquinolin-4-yl)methyl]-7-isobutyl-3-(4-methyl-4H-1,2,4-triazol-3-yl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione

Participants

Role	Name	HCID	Charge
Reactant	6-Chloroquinoline-4-carbaldehyde	HCID 3146031	—
Reactant	4-methyl-4H-1,2,4-triazole-3-carbaldehyde	HCID 15707895	—
Reactant	6-hydrazino-1-isobutylpyrimidine-2,4(1H,3H)-dione	HCID 69428077	—
Product	2-[(6-chloroquinolin-4-yl)methyl]-7-isobutyl-3-(4-methyl-4H-1,2,4-triazol-3-yl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione	HCID 58981083	—

Reaction Steps

This compound was made following the procedure described above, starting with 6-hydrazino-1-isobutylpyrimidine-2,4(1H,3H)-dione, and condensing first with 6-chloroquinoline-4-carbaldehyde, followed by 4-methyl-4H-1,2,4-triazole-3-carbaldehyde. 460.2 (M+H).

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US07285558B2
Source dataset	uspto-grants-2007_10
ORD ID	ord-22b6767e484149e09c84a3e33a57bf01
Source note	uspto-grants-2007_10