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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197524Generated: November 2, 2026

Formamidine acetate → HCID 57758181, compound

https://huagongshe.com/reaction/2197524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
Reactantethyl 1-amino-4-(4-amino-3-fluorophenyl)-5-cyano-1H-pyrrole-3-carboxylateHCID 66786981—
Solvent1-ButanolHCID 263—
ProductHCID 57758181HCID 5775818185.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

Formamidine acetate (22.4 g, 215 mmol) was added to a suspension of ethyl 1-amino-4-(4-amino-3-fluorophenyl)-5-cyano-1H-pyrrole-3-carboxylate (6.2 g, 21.5 mmol) in n-butanol (100 mL). The reaction was heated (100° C.) for 16 h and then cooled to rt. The solvent was removed under reduced pressure and then ethanol (50 mL) and water (200 mL) were added. The mixture was stirred for 30 min and the resulting precipitate was collected by filtration. The solid was washed with water (2×50 mL) and dried to afford desired product (5.80 g, 85%); 1H NMR (300 MHz, DMSO-d6) δ 8.08 (s, 1H), 8.00-8.10 (br s, 1H), 7.90 (s, 1H), 7.03 (dd, J=12.3, 1.9 Hz, 1H), 6.77-6.88 (m, 2H), 5.36 (s, 2H), 5.21-5.31 (br s, 1H), 4.06 (q, J=7.1 Hz, 2H), 1.11 (t, J=7.1 Hz, 3H); ES-MS m/z 316.4 (MH)+; HPLC RT (Method B) 2.39 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338594B2
Source datasetuspto-grants-2012_12
ORD IDord-5f6fb708a09b4f8888c184a1931bb29e
Source noteuspto-grants-2012_12