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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371488Generated: November 3, 2026

Chloroacetonitrile → HCID 21936064, compound

https://huagongshe.com/reaction/1371488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantHCID 21935986HCID 21935986—
ProductHCID 21936064HCID 21936064—

Reaction Steps

Using an analogous procedure to that described in Example 12, 4-(6-chloro-2,3-methylenedioxyanilino)-6-methoxy-7-(piperidin-4-ylmethoxy)quinazoline was reacted with 2-chloroacetonitrile to give the title compound as a solid; NMR Spectrum: (DMSOd6) 1.65 (m, 2H), 2.1 (m, 2H), 2.2 (m, 1H), 3.15 (m, 2H), 3.6 (m, 2H), 4.05 (s, 3H), 4.15 (m, 2H), 4.55 (s, 2H), 6.15 (s, 2H), 7.05 (d, 1H), 7.15 (d, 1H), 7.4 (s, 1H), 8.15 (s, 1H), 8.9 (s, 1H); Mass Spectrum: M−H− 480 and 482.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157467B2
Source datasetuspto-grants-2007_01
ORD IDord-3487ec9d5887476abad3ad084401b58d
Source noteuspto-grants-2007_01