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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453640Generated: October 30, 2026

Triethylamine → HCID 66701951, compound

https://huagongshe.com/reaction/453640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66674947HCID 66674947—
ReactantHCID 86631187HCID 86631187—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66701951HCID 66701951121.8%

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 numberUS08492399B2
Source datasetuspto-grants-2013_07
ORD IDord-797976431bca4a5da60503afa3f76f1d
Source noteuspto-grants-2013_07