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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561952Generated: October 31, 2026

Hydrochloric Acid → HCID 136200335, compound

https://huagongshe.com/reaction/561952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66793557HCID 66793557—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Solvent1,4-DioxaneHCID 31275—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 136200335HCID 13620033538%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 3-(5-amino-6-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-azetidine-1-carboxylic acid tert-butyl ester (830 mg, 2.2 mmol) and 10% Pd/C (85 mg) was added 2-propanol (10 mL), and then MeOH (90 mL). After it was stirred under atmospheric hydrogen for 4 h, the reaction mixture was filtered over Celite. The filtrate was mixed with 4-iodo-2-methoxynicotinic aldehyde (580 g, 2.2 mmol) and HOAc (5.0 mL), stirred at the room temperature for 18 h, and evaporated under reduced pressure to afford an oil crude which was mixed with HCl in dioxane (4 M, 30 mL) and H2O (2.5 mL), heated at 70° C. for 2.5 h and evaporated at 95° C. (the bath temperature) to dryness. The residue was diluted with a mixed solvent of DCM/MeOH (30 mL/70 mL), basified with 28% aqueous NH4OH and concentrated. Chromatography of the crude with CH2Cl2/MeOH/28% aqueous NH4OH (25:10:1) afforded a crude product which was mixed with HOAc (2.1 mL) and HCHO (37% in H2O, 2.1 mL) in a mixed solvent of MeOH/THF (24 mL/24 mL). The resulting reaction mixture was stirred at the room temperature for 10 min and followed by addition of Na(OAc)3BH (2.54 g, 12.0 mmol). The reaction mixture was stirred at the room temperature for 63 h and then evaporated. Chromatography of the residue with CH2Cl2/MeOH/28% aqueous NH4OH (90:10:1) afforded the title compound (330 mg, 38%). ESI-MS m/z 398.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063225B2
Source datasetuspto-grants-2011_11
ORD IDord-cbb5e30f8dab4ed8a262a40a9bd85075
Source noteuspto-grants-2011_11