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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244327Generated: November 1, 2026

N-methyl-2-pyrrolidone → HCID 21919247, compound

https://huagongshe.com/reaction/1244327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantPiperidin-4-olHCID 79341—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178491999HCID 178491999—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 21919247HCID 2191924770%

Reaction Conditions

Temperature120 °C

Reaction Steps

0.05 g 5-Chloro-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3H-imidazo[4,5-b]pyridine (0.11 mmol), 0.034 g 4-hydroxypiperidine (0.34 mmol), 1 mg DMAP and 0.4 ml Hünigs base (2.2 mmol) were dissolved in NMP (1 ml). After stirring for 72 h at 120° C., the reaction mixture was concentrated and the residue taken up in water. A precipitation formed, which was filtered and dried in vacuo to yield 0.04 g 1-[3-methoxymethyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3H-imidazo[4,5-b]pyridin-5-yl]-piperidin-4-ol (70%) as a light brown solid; M.p.: 120–130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122545B2
Source datasetuspto-grants-2006_10
ORD IDord-23ac63f6ae5849f792a206574363a4c4
Source noteuspto-grants-2006_10