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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846603Generated: November 3, 2026

Diisopropylethylamine → HCID 66905552, compound

https://huagongshe.com/reaction/1846603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl N-(3-oxopropyl)carbamateHCID 10910051—
ReactantHCID 66674619HCID 66674619—
SolventDichloromethaneHCID 6344—
ProductHCID 66905552HCID 66905552100%

Reaction Steps

trans-7-Amino-8,8-dimethyl-6-methoxy-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid amide hydrochloride (0.75 g, 2.64 mmol), (3-oxo-propyl)-carbamic acid tert-butyl ester (0.55 g, 3.16 mmol), and N,N-diisopropylethylamine (1.38 mL, 7.92 mmol) were dissolved in dichloromethane (15 mL) at room temperature. Sodium triacetoxyborohydride (1.03 g, 4.85 mmol) was added and the reaction was stirred for 17 h at room temperature. Saturated sodium bicarbonate was added, and the reaction mixture was extracted with dichloromethane. The organic extract was dried with Na2SO4 and concentrated to give the title compound as the crude free base (1.07 g, 100% yield, 79% purity). (m/z): [M+H]+ calcd for C22H35N3O4, 406.3; found, 406.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952031B2
Source datasetuspto-grants-2015_02
ORD IDord-1ff1aacdd8e4484f9e3ff25ce00f4f84
Source noteuspto-grants-2015_02