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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597108Generated: November 3, 2026

HCID 86757422, compound → HCID 18536864, compound

https://huagongshe.com/reaction/1597108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86757422HCID 86757422—
ReactantHCID 86757424HCID 86757424—
ProductHCID 18536864HCID 1853686488%

Reaction Steps

4-(2-{[2-(Methylethyl)phenyl]amino{(1,3-thiazol-4-yl))-5-methylthiothiophene-2-carboxamidine hydrochloride: Methyl 4-(2-{[2-(methylethyl)phenyl]amino}(1,3-thiazol-4-yl))-5-methylthiothiophene-2-carboxylate hydrobromide (33.1 mg, 0.06 mmol) was treated as described in Example 154, step (b) to give 22.4 mg (88%) of 4-(2-{[2-(methylethyl)phenyl]amino}(1,3-thiazol-4-yl))-5-methylthiothiophene-2-carboxamidine hydrochloride. 1H NMR (DMSO-d6, 300 MHz) δ 1.19 (d, 6H, J=6.8 Hz), 2.70 (s, 3H), 3.32 (m, 1H), 7.04 (s, 1H), 7.14-7.25 (m, 2H), 7.35 (dd, 1H, J=1.4, 7.5 Hz), 7.86 (dd, 1H, J=1.4, 7.9 Hz), 8.37 (s, 1H); Mass Spectrum (ESI) m/z calcd. for C18H20N4S3, 388.58 (M+H), found 389.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291514B1
Source datasetuspto-grants-2001_09
ORD IDord-49d9e83e2586405b8ccce13b65ce9a8c
Source noteuspto-grants-2001_09