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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692217Generated: November 2, 2026

Formaldehyde → HCID 57494824, compound

https://huagongshe.com/reaction/1692217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 46841354HCID 46841354—
SolventDichloromethaneHCID 6344—
ProductHCID 57494824HCID 57494824—

Reaction Steps

4-[2-(1-Azetidin-3-yl-1H-pyrazol-5-yl)-4-fluorophenoxy]-5-chloro-2-flouro-N-1,3-thiazol-4-ylbenzenesulfonamide (Example 808, 29 mg, 0.052 mmol) was stirred in dichloromethane (2 ml), methanol (0.2 ml), aqueous formaldehyde (0.015 ml of 37% wt/vol) added and the reaction stirred at room temperature for a further 30 minutes. Sodium triacetoxyborohydride (37 mg, 0.172 mmol) was added and the solution stirred for 3 hours. The solvents were removed in vacuo and the residue dissolved in ethyl acetate and extracted with saturated aqueous sodium hydrogencarbonate solution (2×10 ml) and brine (2×10 ml). The organic layer was separated, dried over sodium sulphate, filtered and evaporated to give a solid. The compound was purified using preparative HPLC to afford the title compound. Yield 15.9 mg 57%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153814B2
Source datasetuspto-grants-2012_04
ORD IDord-eabb7bcadf9349e9b09cae9cb7564151
Source noteuspto-grants-2012_04