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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098778Generated: October 31, 2026

4-(Chloromethyl)pyridine → HCID 86618427, compound

https://huagongshe.com/reaction/2098778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)pyridineHCID 74571—
Reactant(2-Chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methanolHCID 46180605—
ReactantHCID 59593094HCID 59593094—
SolventDimethylformamideHCID 6228—
SolventSodium hydrideHCID 24758—
ProductHCID 86618427HCID 86618427—

Reaction Steps

Following the procedures for compound 314, (2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-yl)-methanol in DMF and sodium hydride was alkylated with 4-picolyl chloride to give 4-(2-chloro-6-((pyridin-4-ylmethoxy)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholine. Suzuki coupling of 4-(2-chloro-6-((pyridin-4-ylmethoxy)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholine and 7 was carried out via General Procedure A. Purification using column chromatography gave 320. NMR: CDCl3: 3.90-3.94 (4 H, m, CH2), 4.08-4.13 (4 H, m, CH2), 4.68 (2 H, s, CH2), 4.92 (2 H, s, CH2), 7.30 (2 H, d, J 5.81, Ar), 7.46 (1 H, s, Ar), 7.51 (1 H, t, J 8.14, Ar), 7.60 (1 H, d, J 8.20, Ar), 8.28 (1 H, d, J 7.32, Ar), 8.61 (2 H, d, J 5.27, Ar), 9.01 (1 H, s, Ar) and 10.14 (1 H, s, NH). MS: (ESI+): MH+ 459.17

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-9437d7e5f3e24df3af33880503531fae
Source noteuspto-grants-2013_05