HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415229Generated: October 30, 2026
Sodium triacetoxyborohydride → HCID 11352263, compound
https://huagongshe.com/reaction/2415229
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 7-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amine | HCID 10082172 | — |
| Reactant | 5-Oxo-4-(4-oxobutyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester | HCID 11312149 | — |
| Product | HCID 11352263 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818645B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-c76487d4d95b4779b7454ebe69f9fa5b |
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| Source note | uspto-grants-2004_11 |
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