Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827441Generated: October 30, 2026

Formic Acid → N-[2-Fluoro-4-(4-fluoro-benzyloxy)-phenyl]-2-formylamino-acetamide

https://huagongshe.com/reaction/1827441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-amino-N-[2-fluoro-4-(4-fluoro-benzyloxy)-phenyl]-acetamideHCID 10447035—
SolventDichloromethaneHCID 6344—
SolventHCID 178506446HCID 178506446—
ProductN-[2-Fluoro-4-(4-fluoro-benzyloxy)-phenyl]-2-formylamino-acetamideHCID 1033612291%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of acetic anhydride (40 mg, 0.39 mmol) and formic acid (22 mg, 0.48 mmol) was stirred at 0° C. and then heated uat 60° C. for 1 h. Step 2: During this time, 2-amino-N-[2-fluoro-4-(4-fluoro-benzyloxy)-phenyl]-acetamide (1:1) hydrochloride (50 mg, 0.15 mmol) was extracted with DCM and sodium hydrogen carboante (saturated) and the organic layer evaporated. Then to a mixture of the acetic formic anhydride (Step 1) in dry THF (0.5 mL) was added a solution of the amine (Step 2) in dry THF (1 mL) at room temperature and the resulting mixture stirred for 10 min. Then the reaction mixture was evaporated leave the title compound (44.1 mg, 91%) as a white solid. MS: m/e=321.1 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053245B2
Source datasetuspto-grants-2006_05
ORD IDord-b74e85e3a9fc467184f8d856fdd00454
Source noteuspto-grants-2006_05