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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858644Generated: October 30, 2026

5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehyde → HCID 58762487, compound

https://huagongshe.com/reaction/858644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehydeHCID 23635226—
ReactantHCID 58762314HCID 58762314—
ReactantHCID 86600107HCID 86600107—
ProductHCID 58762487HCID 58762487—

Reaction Steps

The title compound was prepared analogously to Example A(131), where 6-cyclopentyl-6-[2-(4-hydroxy-3-propylphenyl)ethyl]dihydro-2H-pyran-2,4(3H)-dione was substituted in place of 6-cyclopentyl-6-[2-(3-fluoro-4-{methyl[methyl(dimethylene)-sulfanyl]amino}phenyl)ethyl]dihydro-2H-pyran-2,4(3H)-dione and 5,7-diethyl[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehyde was substituted in place of 5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carbaldehyde. 1H NMR (CDCl3): δ 1.00 (t, J=7.54 Hz, 3H), 1.40–1.80 (brm, 16H), 2.00–2.18(m, 5H), 2.59 (m, 2H), 2.73 (m, 4H), 2.95 (m, 2H), 4.00 (s, 2H), 6.67 (d, J=5.78 Hz, 1H), 6.95 (m, 2H), 7.21 (s, 1H). Anal. Calcd. For C32H40O4N4: C, 70.56; H, 7.40; N, 10.29. Found: C, 70.23; H, 7.69; N, 10.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-b80f11178754412aa0b529adeb6c18c7
Source noteuspto-grants-2006_12