Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731748Generated: October 31, 2026

HCID 49841325, compound → HCID 49841328, compound

https://huagongshe.com/reaction/731748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 49841325HCID 49841325—
ReactantHCID 178480876HCID 178480876—
ProductHCID 49841328HCID 49841328—

Reaction Steps

[4-(2-Isopropyl-pyrazolo[1,5-a]pyridin-3-yl)-pyrimidin-2-yl]-[3-(4-methyl-piperazin-1-yl)-propyl]-amine was prepared from 3-dimethylamino-1-(2-isopropyl-pyrazolo[1,5-a]pyridin-3-yl)-propenone and N-[3-(4-methyl-piperazin-1-yl)-propyl]-guanidine following the method used in Step 4 of the synthesis of Isopropyl-[4-(2-isopropylpyrazolo[1,5-a]pyridin-3-yl)-pyrimidin-2-yl]-amine (Example 66), except preparative-HPLC purification was used in the place of recrystallization (162 mg, 19%). 1H-NMR (250 MHz, DMSO-d6) δ 8.72 (d, J=6.8 Hz, 1H), 8.28-8.20 (m, 2H), 7.37 (t, J=7.8 Hz, 1H), 7.16-7.10 (m, 1H), 6.99 (t, J=6.6 Hz, 1H), 6.80 (d, J=7.3 Hz, 1H), 3.78 (sept, J=7.3 Hz, 1H), 2.56-2.32 (m, 10H), 2.22 (s, 3H), 2.10-2.06 (m, 2H), 1.73 (pent, J=6.9 Hz, 2H), 1.35 (d, J=6.8 Hz, 6H); LC/MS 394.3 m/z (M+H+). Compound 1135.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585875B2
Source datasetuspto-grants-2009_09
ORD IDord-70884615d78f40d2a19cd23c6cba4153
Source noteuspto-grants-2009_09