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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440028Generated: November 1, 2026

Hydrochloric Acid → HCID 86748388, compound

https://huagongshe.com/reaction/1440028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium AzideHCID 33557—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 86748390HCID 86748390—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 86748388HCID 8674838872.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3β-[3'-iodo-4'-aminophenyl]tropan-2β-carboxylic acid methyl ester dihydrochloride (1a) (90 mg, 0.1902 retool) in 1 mL of AcOH (3M) was added an aqueous solution of NaNO2 (17.3 mg, 0.2661 mmol, in 0.5 mL of H2O) at 0° C. After 30 min at this temperature NaN3 (19 mg, 0.2754 mmol) in 0.5 mL of H2O was added dropwise to the reaction mixture and stirred for 30 min at 0° C. then 30 min at room temperature. After removal of all solvent by evaporation, the residue was dissolved in CHCl3 and washed with H2O. The organic layer was dried over MgSO4 and concentrated to give an oil which was converted to HCl salt to yield 64 mg (72.7%) of 3β-[3'-iodo-4'-azidophenyl]tropan-2β-carboxylic acid methyl ester hydrochloride (1b) as a yellowish solid: mp 140°-143° C.; [α] 25 -97.4° (c 0.115), MeOh); 1H NMR (250 MHz, CDCl3) δ 1.51-1.73 (m, 3) 2.07-2.16 (m, 2), 2.19 (s, 3, NCH3) 2.47 (m, 1), 2.80-2.93 (m, 2), 3.32 (m, 1, H-5), 3.51 (s, 3, OCH3), 3.54 (m, 1, H-1), 7.01 (d, 1, J-7.7, ArH), 7.28 (dd, 1, J=7.77, J=1, ArH), 7.60 (d, 1, J=1, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05496953
Source datasetuspto-grants-1996_03
ORD IDord-0f47dca94ab14e75b54a2de42453f59c
Source noteuspto-grants-1996_03