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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177548Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 44599682, compound

https://huagongshe.com/reaction/1177548

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantBenzylamineHCID 7504—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86638722HCID 86638722—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 44599682HCID 44599682—

Reaction Steps

2-(3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)phenyl)acetaldehyde (44 mg, 0.113 mmol) was dissolved in chloroform (1.1 mL) before it was stirred at ambient temperature with benzylamine (62 μl, 0.57 mmol) and PTSA (1 mg) for 16 h. Methanol (1.1 mL) and sodium cyanoborohydride (7.1 mg, 0.113 mmol) were then added and allowed to stir in the reaction mixture over 3 d. The reaction mixture was diluted with DCM, added to a separatory funnel, partitioned with sodium bicarbonate (saturated, aqueous), washed with sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, and concentrated via rotovap to give the title compound after flash chromatography. MS (ESI) m/z: Calculated: 479.2; Observed: 480.1 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842685B2
Source datasetuspto-grants-2010_11
ORD IDord-ad78e595aee64e0e96e46ec8d40444a8
Source noteuspto-grants-2010_11