Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371794Generated: November 2, 2026

Methanesulfonyl chloride → HCID 21070483, compound

https://huagongshe.com/reaction/1371794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 21070476HCID 21070476—
ProductHCID 21070483HCID 21070483—

Reaction Steps

The similar procedure as described in Example 60 was used, starting from [4-amino-2-(4-amino-cyclohexylamino)-pyrimidin-5-yl]-(5-fluoro-2-methoxy-4-methyl-phenyl)-methanone (Example 345) and methanesulfonyl chloride (Aldrich) to give N-[4-[4-amino-5-(5-fluoro-2-methoxy-4-methyl-benzoyl)-pyrimidin-2-ylamino]-cyclohexyl]-methanesulfonamide. MS (M+H)+, 452.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157455B2
Source datasetuspto-grants-2007_01
ORD IDord-2a2117665eec4443b15eb1b558f3ba70
Source noteuspto-grants-2007_01