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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227392Generated: October 31, 2026

Triethylamine → HCID 18473236, compound

https://huagongshe.com/reaction/2227392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 18473242HCID 18473242—
ReactantHCID 18473245HCID 18473245—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 18473236HCID 18473236—

Reaction Steps

3-(Piperazin-1-ylsulfonyl) phenol hydrochloride (0.065 g, 0.231 mmol) was dissolved in MeOH (5 mL), neutralized with Et3N (0.032 mL, 0.231 mmol), then treated with N-[1-(4-cyano-3-fluorophenyl)-4-oxo-1-(1-methyl-1H-imidazol-5-yl)butyl]-2-methylpropane-2-sulfinamide (0.086 g, 0.220 mmol). The pH of the solution was adjusted to 5 with HOAc, then NaCNBH3 (0.021 g, 0.330 nunol) was added, and the pH was adjusted again to 5. After stirring at ambient temperature for 18 h, the reaction mixture was concentrated in vacuo, partitioned between CH2Cl2 and aqueous saturated NaHCO3 solution, the aqueous layer washed with CH2Cl2 (2×), the organic layers combined and dried (MgSO4), filtered and concentrated to give the title product. MS(M+1) 617.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413964B1
Source datasetuspto-grants-2002_07
ORD IDord-e02af881543c4e63b1c4d08aa19aa634
Source noteuspto-grants-2002_07