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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815930Generated: October 31, 2026

Diisopropylethylamine → N-{5-[4-(1-benzyl-1H-indazol-5-ylamino)-[1,3,5]triazin-2-ylamino]-2-methoxyphenyl}-acrylamide

https://huagongshe.com/reaction/1815930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(5-amino-2-methoxyphenyl)-acrylamideHCID 22496104—
Reactant(1-benzyl-1H-indazol-5-yl)-(4-chloro-[1,3,5]triazin-2-yl)amineHCID 22496107—
ProductN-{5-[4-(1-benzyl-1H-indazol-5-ylamino)-[1,3,5]triazin-2-ylamino]-2-methoxyphenyl}-acrylamideHCID 10300180—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a slurry of (1-benzyl-1H-indazol-5-yl)-(4-chloro-[1,3,5]triazin-2-yl)-amine (Example 3, Step 3) (90 mg, 0.267 mmol) in IpOH (3 ml) was added DIEA (0.070 mL, 0.401 mmol) and N-(5-amino-2-methoxyphenyl)acrylamide (Step 2) (56.5 mg, 0.294 mmol). The mix was heated at 100° C. for 18 h. The solution was then cooled to RT. A precipitate fell out of solution, was filtered off and dried under reduced pressure to give N-{5-[4-(1-benzyl-1H-indazol-5-ylamino)-[1,3,5]triazin-2-ylamino]-2-methoxyphenyl}-acrylamide: MS m/z=493[M+H]+. Calc'd for C27H24N8O2: 492.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881737B2
Source datasetuspto-grants-2005_04
ORD IDord-bfc8c9f648004d2e96e3cbb5fb8f3f76
Source noteuspto-grants-2005_04