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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415229Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 11352263, compound

https://huagongshe.com/reaction/2415229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant7-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amineHCID 10082172—
Reactant5-Oxo-4-(4-oxobutyl)-[1,4]diazepane-1-carboxylic acid tert-butyl esterHCID 11312149—
ProductHCID 11352263HCID 11352263—

Reaction Steps

To a solution of (7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine prepared as described in Example 1 (800 mg, 3.3 mmol, 1 eq) in 1,2-dichlororethane (40 mL) under inert atmosphere was added 5-oxo-4-(4-oxo-butyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester (1.0 g, 3.6 mmol, 1.1 eq.) in a single portion followed by the sodium triacetoxyborohydride (1.7 g, 8.25 mmol, 2.5 eq.). The reaction was stirred at room temperature for 20 hr, concentrated in-vacuo and then partitioned between 10% KOH (50 mL) and ethyl acetate (100 mL). The organic layer was washed with brine, dried (MgSO4) and concentrated. Purification by silica gel chromatography gave 1.1 g of 4-{4-[(7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-butyl}-5-oxo-[1,4]diazepane-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818645B2
Source datasetuspto-grants-2004_11
ORD IDord-c76487d4d95b4779b7454ebe69f9fa5b
Source noteuspto-grants-2004_11