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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241968Generated: October 29, 2026

3-(Methylthio)propylamine → HCID 58083233, compound

https://huagongshe.com/reaction/241968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylthio)propylamineHCID 77743—
Reactant4-Chloro-6-(1H-indazol-4-yl)-1-methyl-1H-pyrazolo[3,4-b]pyridineHCID 58083234—
ProductHCID 58083233HCID 58083233—

Reaction Steps

4-Chloro-6-(1H-indazol-4-yl)-1-methyl-1H-pyrazolo[3,4-b]pyridine 7 (100 mg) and 3-(methylthio)propylamine (3 equiv.) were heated in microwave at 170° C. for one hour following General Procedure B. Volatiles were removed in vacuo; the residue was purified by prep HPLC to give [6-(1H-indazol-4-yl)-1-methyl-1H-pyrazolo[3,4-b]pyridin-4-yl]-(3-methylsulfanyl-propyl)-amine (94 mg) as a white solid. 3-Chloroperoxybenzoic acid (MCPBA, 94 mg, 2.2 equiv.) in 2 ml dry DCM was added at 0° C. The reaction mixture was allowed slowly to warm up to room temperature over 3 hours and extracted with DCM, washed with saturated aqueous sodium hydrogen carbonate and purified by flash chromatography (methanol/DCM) to give 116 (27 mg) as a white solid. NMR (CDCl3): 2.39 (2H, m), 3.00 (3H, s), 3.25 (2H, t), 3.74 (2H, m), 4.20 (3H, s), 5.20 (1H, br t), 6.77 (1H, s), 7.50-7.54 (1H, m), 7.59 (1H, d), 7.70 (1H, d), 7.97 (1G=H, s), 8.82 (1H, s), 10.20 (1H, br). MS: MH+ 385.19 (100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653098B2
Source datasetuspto-grants-2014_02
ORD IDord-d029b225cf5a4639a93f0663afc75834
Source noteuspto-grants-2014_02