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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880811Generated: November 1, 2026

Triethylamine → HCID 66702020, compound

https://huagongshe.com/reaction/1880811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66674947HCID 66674947—
ReactantHCID 86631187HCID 86631187—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66702020HCID 66702020125.8%

Reaction Steps

(6S,7S)-7-Amino-8,8-diethyl-6-methoxy-5,6,7,8-tetrahydro-naphthalen-2-ol hydrochloride salt (100 mg, 0.35 mmol), (R)-2-cyclohexylmethyl-4-oxo-butyric acid methyl ester (90 mg, 0.42 mmol) and triethylamine (35 mg, 0.035 mmol) were dissolved in dichloromethane (2.0 mL) and stirred at room temperature for 30 min. Sodium triacetoxyborohydride (1.03 g, 4.85 mmol) was added and the reaction was monitored by HPLC. After 3 h, additional (R)-2-cyclohexylmethyl-4-oxo-butyric acid methyl ester (20 mg, 0.1 mmol) and sodium triacetoxyborohydride (30 mg, 0.14 mmol) were added. Thirty minutes after the last addition, EtOAc (15 mL) was added and the mixture was washed with 5% aqueous sodium carbonate (2×5 mL) and saturated sodium chloride (5 mL). The organic layer was dried with Na2SO4) and concentrated to give the title compound (190 mg). (m/z): [M+H]+ calcd for C27H43NO4, 446.33. found, 446.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318765B2
Source datasetuspto-grants-2012_11
ORD IDord-2577f12d55d54ac2931d49c04f41e129
Source noteuspto-grants-2012_11