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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867395Generated: November 2, 2026

Borane;pyridine → 4-[3-((-)-4-Hydroxy-6-aza-spiro[2.5]oct-6-yl)-propyl]-5-oxo-[1,4]diazepane-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1867395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;pyridineHCID 2723995—
Reactant6-Azaspiro[2.5]octan-4-OL hydrochlorideHCID 66783582—
Reactant5-Oxo-4-(3-oxo-propyl)-[1,4]diazepane-1-carboxylic acid tert-butyl esterHCID 86615868—
SolventAcetic AcidHCID 176—
Solvent1,2-Dichloroethane ethanolHCID 22901612—
Product4-[3-((-)-4-Hydroxy-6-aza-spiro[2.5]oct-6-yl)-propyl]-5-oxo-[1,4]diazepane-1-carboxylic acid tert-butyl esterHCID 6844028493.6%

Reaction Steps

5-Oxo-4-(3-oxo-propyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester (intermediate 61) (0.19 g, 0.7 mmol) was reacted with (−)-6-Aza-spiro[2.5]octan-4-ol hydrochloride (intermediate 83) (0.12 g, 0.7 mmol) in DCE:EtOH (1:1, 6 ml), AcOH (0.18 ml) and pyridine-borane complex (0.18 ml, 8M in pyridine, 1.4 mmol) for 20 minutes. The reaction was then concentrated, redissolved in CH2Cl2 and washed with sat. NaHCO3, dried (Na2SO4) and concentrated. The residue was purified by flash column chromatography (CH2Cl2:MeOH 8:2) to afford the title product (0.25 g, 91%) as a gum. MS: 382.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632829B2
Source datasetuspto-grants-2009_12
ORD IDord-fab9f11bec2245bc84c52135b74d683b
Source noteuspto-grants-2009_12