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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040924Generated: October 31, 2026

2-(2,5-Dichloropyrimidin-4-ylamino)-N-methylbenzamide → N-Methylbenzamide

https://huagongshe.com/reaction/1040924

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2,5-Dichloropyrimidin-4-ylamino)-N-methylbenzamideHCID 57974132—
ReactantHCID 67264199HCID 67264199—
SolventTrifluoroacetic acidHCID 6422—
ProductN-MethylbenzamideHCID 11954204.9%

Reaction Conditions

Temperature115 °C

Reaction Steps

A solution of 3,4-dihydro-2H-benz[b][1,4]dioxepin-ylamine (0.024 g, 0.00015 mol) and 2-(2,5-dichloro-pyrimidin-4-ylamino)-N-methylbenzamide (0.04 g, 0.00013 mol) in TFA (0.5 mL) was evaporated and then heated to 115° C. for 15 min. Purification by ISCO chromatography gave 2-[5-chloro-2-(3,4-dihydro-2H-benzo[b]1,4]dioxepin-2-ylamino)-pyrimidin-4-ylamino]-N-methyl-benzamide (0.036 g, 56%) vas a white solid. MP: 214-5° C.; 1H-NMR (DMSO-d6) δ 11.58 ((s, 1H), 9.36 (s, 1H), 8.74 (m, 2H), 8.20-1 (s, 1H), 7.74-6 (d, 1H), 7.50-2 (m, 1H), 7.42-8 (s, 1H), 7.14-6 (m, 2H), 6.86-8 (d, 1H), 4.05 (d, 2H), 4.09 (d, 2H), 2.81 (s, 3H), 2.07 (s, 2H); (LC/MS (ESI+): 426 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-ac7b4c65df834bd09021364a32f03534
Source noteuspto-grants-2013_10