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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917201Generated: October 30, 2026

4-(3-(Dimethylamino)propyl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-7-amine → HCID 178483516, compound

https://huagongshe.com/reaction/1917201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-(Dimethylamino)propyl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-7-amineHCID 59144093—
ReactantMethyl thiophene-2-carbimidothioate hydroiodideHCID 66704664—
SolventEthanolHCID 702—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178483516HCID 17848351686%

Reaction Steps

A solution of 4-(3-(dimethylamino)propyl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-7-amine (0.22 g, 0.875 mmol) in dry ethanol (10 mL) was treated with methyl thiophene-2-carbimidothioate hydroiodide (0.499 g, 1.750 mmol) at room temperature, and the resulting mixture was stirred over night (18 hours) at room temperature. The reaction was diluted with saturated NaHCO3 solution (25 mL), and the product was extracted into CH2Cl2 (3×20 mL). The combined CH2Cl2 layers were washed with brine (15 mL) and dried (Na2SO4). The solvent was evaporated, and the crude material was purified by column chromatography (5:95 (2M NH3 in MeOH):CH2Cl2) on silica gel to obtain the title product 22 (0.27 g, 86%) as a solid. 1H NMR (DMSO-d6) δ 7.68 (d, 1H, J=3.0 Hz), 7.56 (d, 1H, J=5.1 Hz), 7.06 (dd, 1H, J=3.9, 4.8 Hz), 6.69 (d, 1H, J=8.7 Hz), 6.52-6.45 (m, 2H), 6.33 (brs, 2H), 3.51-3.48 (m, 2H), 3.25 (t, 2H, J=7.2 Hz), 3.04-3.01 (m, 2H), 2.25 (t, 2H, J=6.9 Hz), 2.14 (s, 6H), 1.70-1.61 (m, 2H); ESI-MS (m/z, %): 361 (MH+, 93), 276 (100); HPLC purity: 98.23% by area.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618286B2
Source datasetuspto-grants-2013_12
ORD IDord-3d479c4648e04512825010f74743b9bd
Source noteuspto-grants-2013_12