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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475305Generated: October 30, 2026

1-(1h-Indol-5-yl)ethylamine adipate → N2-((4-chloro-1H-indol-5-yl)methyl)-N4-(5-cyclopropyl-1H-pyrazol-3-yl)-6-methylpyrimidine-2,4-diamine

https://huagongshe.com/reaction/475305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1h-Indol-5-yl)ethylamine adipateHCID 52993441—
Reactant2-chloro-N-(3-cyclopropyl-1H-pyrazol-5-yl)-6-methylpyrimidin-4-amineHCID 59819615—
Reactanttert-butyl 5-(aminomethyl)-4-chloro-1H-indole-1-carboxylateHCID 71272344—
ReactantHCID 178478345HCID 178478345—
ProductN2-((4-chloro-1H-indol-5-yl)methyl)-N4-(5-cyclopropyl-1H-pyrazol-3-yl)-6-methylpyrimidine-2,4-diamineHCID 86694737—

Reaction Steps

N2-((4-chloro-1H-indol-5-yl)methyl)-N4-(5-cyclopropyl-1H-pyrazol-3-yl)-6-methylpyrimidine-2,4-diamine (I-19) was prepared using procedure analogous to the preparation of I-8, step 1, except 2-chloro-N-(5-cyclopropyl-1H-pyrazol-3-yl)-6-methyl-pyrimidin-4-amine 185 and tert-butyl 5-(aminomethyl)-4-chloro-1H-indole-1-carboxylate were used in place of 53 and 1-(1H-indol-5-yl)ethanamine adipic acid salt, respectively, to afford I-19; MS (ESI) m/z=394.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637537B2
Source datasetuspto-grants-2014_01
ORD IDord-643f4f5e95d94045b3eaad172b52906f
Source noteuspto-grants-2014_01