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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894478Generated: November 1, 2026

Sodium Bicarbonate → HCID 57670057, compound

https://huagongshe.com/reaction/1894478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthanamine, 2-(methylsulfonyl)-, hydrochloride (1:1)HCID 17749886—
ReactantHCID 57670001HCID 57670001—
SolventDichloromethaneHCID 6344—
ProductHCID 57670057HCID 5767005775%

Reaction Steps

To a solution of 1-[(4S,5R)-2-(6-tert-butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl]-piperidin-4-one (64.6 mg, 0.104 mmole, example 209) and 2-aminoethyl methylsulfone hydrochloride (17.9 mg, 0.112 mmole, Array) in dichloromethane (3 mL) were added sodium acetate (21.1 mg, 0.257 mmole) and sodium triacetoxyborohydride (40.1 mg, 0.189 mmole). The mixture was stirred at room temperature overnight before saturated solution of sodium bicarbonate (3 mL) was added. After stirred for 1 h, the mixture was extracted with dichloromethane (2×10 mL). The combined organic extracts were washed with brine, dried over sodium sulfate and concentrated to dryness. The crude product was purified by flash column chromatography (silica gel, eluting with a gradient of 1% to 10% methanol in dichloromethane) to give the title compound (56.7 mg, 75% yield). HR-MS (ES, m/z) calculated for C37H48Cl2N5O4S [(M+H)+] 728.2799, observed 728.2796.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513239B2
Source datasetuspto-grants-2013_08
ORD IDord-b613d1607f434565a2fda2e77fff8d31
Source noteuspto-grants-2013_08