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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049930Generated: October 30, 2026

3-Methylbenzylamine → HCID 72703926, compound

https://huagongshe.com/reaction/1049930

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbenzylamineHCID 66015—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86703928HCID 86703928—
SolventDimethylacetamideHCID 31374—
ProductHCID 72703926HCID 7270392620.7%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a microwave vial was added tert-butyl N-tert-butoxycarbonyl-N-(6-chloropyrido[3,2-d]pyrimidin-4-yl)carbamate 50-A (0.20 mmol, 76 mg) followed by 3-methylbenzyl amine (2 equiv., 0.4 mmol, 48 mg), DIPEA (3 equiv., 0.6 mmol, 78 mg), and dimethylacetamide (0.5 mL). The reactions were capped and stirred under microwave irradiation for 30 minutes at 130° C. The reaction was then transferred to an 8 ml vial, and concentrated via GeneVac. To the crude material was added dichloromethane (0.25 mL) followed by trifluoroacetic acid (0.5 mL). The reaction was capped and shaken at room temperature for one hour. The reaction was then concentrated, and the crude purified by reverse phase HPLC to yield 11 mg of product. 1H NMR (400 MHz, DMSO) δ 8.16-8.11 (s, 1H), 7.69-7.62 (d, J=9.1 Hz, 1H), 7.53-7.46 (t, J=5.5 Hz, 1H), 7.40-7.33 (m, 1H), 7.22-7.11 (m, 3H), 7.11-7.07 (d, J=9.1 Hz, 1H), 4.70-4.62 (d, J=5.5 Hz, 2H), 2.37-2.33 (s, 3H). LCMS M/Z (M+H)=266.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382241B2
Source datasetuspto-grants-2016_07
ORD IDord-8fc56336e8fb4ed9869c78a14979a810
Source noteuspto-grants-2016_07