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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412974Generated: October 31, 2026

HCID 86583848, compound → HCID 18537254, compound

https://huagongshe.com/reaction/412974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86583848HCID 86583848—
ReactantHCID 86758976HCID 86758976—
ProductHCID 18537254HCID 1853725447%

Reaction Steps

4-{2-(4-Cyclohexylphenyl)amino(1,3-thiazol-4-yl)}-5-methylthiothiophene-2-carboxamidine hydrochloride: Methyl 4-{2-[(4-cyclohexylphenyl)amino](1,3-thiazol-4-yl)}-5-methylthiothiophene-2-carboxylate hydrobromide (31.1 mg, 0.059 mmol) was treated as described in Example 154, step (b) to give 12.8 mg (47% yield) of 4-{2-[(4-cyclohexylphenyl)amino](1,3-thiazol-4-yl)}-5-methylthiothiophene-2-carboxamidine hydrochloride. 1H NMR (DMSO-d6, 300 MHz) δ 1.33-1.40 (m, 5H), 1.68-1.79 (m, 5H), 2.44 (m, 1H), 2.73 (s, 3H), 7.12 (s, 1H), 7.18 (d, 2H, J=8.7 Hz), 7.68 (d, 2H, J=8.7 Hz), 8.47 (s, 1H), 8.85 (bs, 2H), 9.32 (bs, 2H), 10.28 (s, 1H); Mass Spectrum (ESI) m/z calcd. for C21H24N4S3, 428.64 (M+H), found 429.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562840B1
Source datasetuspto-grants-2003_05
ORD IDord-6bf270b9b0d8459a9a9056cdaba04181
Source noteuspto-grants-2003_05