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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17192Generated: October 26, 2026

Trifluoroacetic acid → 3-(4-Amino-3-methoxyphenyl)-7-iodofuro[3,2-c]pyridin-4-amine

https://huagongshe.com/reaction/17192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-(4-amino-7-iodofuro[3,2-c]pyridin-3-yl)-2-methoxyphenylcarbamateHCID 18451460—
SolventDichloromethaneHCID 6344—
Product3-(4-Amino-3-methoxyphenyl)-7-iodofuro[3,2-c]pyridin-4-amineHCID 1845070980.3%

Reaction Steps

Tert-butyl 4-(4-amino-7-iodofuro[32-c]pyridin-3-yl)-2-methoxyphenylcarbamate (3.98 g 8.28 mmol) was added to a 20% solution of trifluoroacetic acid in dichloro-methane (150 mL). The mixture was stirred for two hours and then the solvent was removed in vacuo. To the residue was added water (15 mL) and dichloromethane (25 mL). The mixture was adjusted to pH 12 with 1 N aqueous sodium hydroxide and the layers were separated. The aqueous layer was extracted with dichloromethane (2×10 mL) and the combined organic layers were dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to give the title compound (2.534 g, 80%). 1H NMR (DMSO-d6, 400 MHz) □ 8.03 (s, 1H) 7.94 (s, 1H) 6.91 (d, 1H) 6.82 (dd, 1H) 6.75 (d, 1H) 5.69-5.77 (bs, 2H) 4.96-5.05 (bs, 2H) 3.81 (s, 3H); RP-HPLC (Conditions f) Rt 11.22 min.; MS: MH+ 382.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-c5daa553e28a4ce2937bcf7b4adf2533
Source noteuspto-grants-2010_06