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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186616Generated: November 1, 2026

(2-Fluorophenyl)thiourea → HCID 86758181, compound

https://huagongshe.com/reaction/2186616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Fluorophenyl)thioureaHCID 2737500—
ReactantMethyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylateHCID 86583828—
ReactantHCID 131723298HCID 131723298—
ProductHCID 86758181HCID 8675818170%

Reaction Steps

Methyl 4-{2-[(2-fluorophenyl)amino](1,3-thiazol-4-yl)}-5-methlylthiothiophene-2-carboxylate hydrobromide: Methyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylate (60 mg, 0.19 mmol) was allowed to react with 2-fluorophenyl thiourea as described in Example 154, step (a) to give 55.6 mg (70% yield) of methyl 4-{2-[(2-fluorophenyl)amino](1,3-thiazol-4-yl)}-5-methylthiothiophene-2-carboxylate hydrobromide. 1H NMR (DMSO-d6, 300 MHz) δ 2.68 (s, 3H), 3.83 (s, 3H), 6.96-7.04 (m, 1H), 7.14-7.29 (m, 3H), 7.35 (s, 1H), 8.06, 8.14 (s, 1H rotomer), 8.61 (td, 1H rotomer, J=1.5, 8.5 Hz), 10.14, 10.30 (s, 1H rotomer); Mass Spectrum (ESI) m/z calcd. for C16H13FN2O2S3, 380.48 (M+H), found 381.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403633B2
Source datasetuspto-grants-2002_06
ORD IDord-a909ae4401434ce19d298c25135af179
Source noteuspto-grants-2002_06