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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847968Generated: November 2, 2026

HCID 86681005, compound → HCID 86681006, compound

https://huagongshe.com/reaction/1847968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86681005HCID 86681005—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
ProductHCID 86681006HCID 8668100699%

Reaction Steps

To a solution of (1R,2R)-2-((6-(hydroxymethyl)benzo[d]thiazol-2-yl)amino)cyclohexanol from Step 1 of this Example (445 mg, 1.6 mmol) in CH2Cl2 (40 mL) was added manganese(IV) oxide (696 mg, 8.0 mmol) at rt. The reaction suspension was heated under reflux overnight. After cooling to rt, the reaction mixture was filtered through a Celite pad. The filtrate was concentrated under reduced pressure to give crude 2-(((1R,2R)-2-hydroxycyclohexyl)amino)benzo[d]thiazole-6-carbaldehyde as a brown oil (440 mg, 99%), which was used to next step without further purification. LCMS (ESI) m/z 277 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-7866b07194bb4a8c9aae2c244d609b6a
Source noteuspto-grants-2015_02