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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058475Generated: November 1, 2026

HCID 86583844, compound → HCID 18537450, compound

https://huagongshe.com/reaction/1058475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86583844HCID 86583844—
ReactantHCID 86758827HCID 86758827—
ProductHCID 18537450HCID 1853745049%

Reaction Steps

4-(2-{[4-(4-Chlorophenoxy)phenyl]amino(1,3-thiazol-4-yl)}-5-methylthiothiophene-2-carboxamidine hydrochloride: Methyl 4-(2-{[4-(4-chlorophenoxy)phenyl]amino}(1,3-thiazol-4-yl))-5-methylthiothiophene-2-carboxylate hydrobromide (300 mg, 0.52 mmol) was treated as described in Example 154, step (b) to give 129.9 mg (49% yield) of 4-(2-{[4-(4-chlorophenoxy)phenyl]amino}(1,3-thiazol-4-yl))-5-methylthiothiophene-2-carboxamidine hydrochloride. 1H NMR (DMSO-d6, 300 MHz) δ 2.72 (s, 3H), 6.97 (m, 2H), 7.07 (m, 2H), 7.15 (s, 1H), 7.40 (m, 2H), 7.85 (m, 2H), 8.46 (s, 1H), 8.82 (bs, 2H), 9.27 (bs, 2H), 10.43 (bss, 1H); Mass Spectrum (ESI) m/z calcd. for C21H17ClN4OS3, 473.1 (M+H), found 473.2, 475.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515002B2
Source datasetuspto-grants-2003_02
ORD IDord-6c63204955464bd7a37c83a28823a695
Source noteuspto-grants-2003_02