Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876932Generated: October 27, 2026

N-(6-chloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N,N',N'-trimethyl-ethane-1,2-diamine → N1-(6-(1H-indazol-4-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N1,N2,N2-trimethylethane-1,2-diamine

https://huagongshe.com/reaction/876932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(6-chloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N,N',N'-trimethyl-ethane-1,2-diamineHCID 58345955—
ReactantHCID 178431105HCID 178431105—
ProductN1-(6-(1H-indazol-4-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N1,N2,N2-trimethylethane-1,2-diamineHCID 44180022—

Reaction Steps

N-(6-chloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N,N′,N′-trimethyl-ethane-1,2-diamine was reacted with indazole boronic acid pinacol ester in General Procedure A. Purification on silica yielded 131. NMR: (CDCl3): 2.38 (s, 6H, 2×CH3), 2.73 (t, 2H, CH2, J=7.17 Hz), 3.54 (s, 311, CH3), 4.08 (m, 2H, CH2), 4.17 (s, 3H, CH3), 7.52 (t, H, ArH, J=7.77 Hz), 7.60 (d, H, ArH, J=8.27 Hz), 8.01 (s, H, ArH), 8.42 (d, H, ArH, J=7.23 Hz), 9.19 (s, H, ArH), 10.35 (sbr, H, NH). MS: (ESI+) MH+=351.18

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987280B2
Source datasetuspto-grants-2015_03
ORD IDord-394236cbafb04800a598c654a4af2301
Source noteuspto-grants-2015_03