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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851775Generated: November 1, 2026

Dimethylformamide → 5-(5-methoxy-1,3-benzothiazol-2-yl)-N-methylpyridin-2-amine

https://huagongshe.com/reaction/1851775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant6-MethoxybenzothiazoleHCID 350186—
Reactant5-Bromopyridine-2-carboxamideHCID 735151—
Reactant6-Methoxy-2-[5-(trifluoromethyl)pyridin-2-yl]-1,3-benzothiazoleHCID 24803891—
CatalystBis(tri-tert-butylphosphine)palladium(0)HCID 2734558—
Product5-(5-methoxy-1,3-benzothiazol-2-yl)-N-methylpyridin-2-amineHCID 24803727—

Reaction Steps

6-Methoxy-1,3-benzothiazole (0.100 g, 0.61 mmol) and 5-bromopyridine-2-carboxamide (0.146 g, 0.73 mmol) were reacted according to the procedure used for the preparation of 6-methoxy-2-[5-(trifluoromethyl)pyridin-2-yl]-1,3-benzothiazole, with the following exceptions: 10 mol % bis(tri-t-butylphosphine) palladium (0) was used and the amount of DMF was reduced (3 mL). The reaction mixture was concentrated and flash chromatography of the residue gave the title compound (10 mg) as an off-white solid. 1H NMR δ 9.25 (dd, 1 H) 8.56 (dd, 1 H) 8.23 (br s, 1 H) 8.19 (dd, 1 H) 8.04 (d, 1 H) 7.81 (d, 1H) 7.78 (br s, 1 H) 7.20 (dd, 1 H) 3.88 (s, 3 H); MS ink (M+H) 286.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957215B2
Source datasetuspto-grants-2015_02
ORD IDord-1f368683f64b428a84477d73c592dfd2
Source noteuspto-grants-2015_02