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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917159Generated: November 1, 2026

4-(2-(Pyrrolidin-1-yl)ethyl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-7-amine → HCID 178511900, compound

https://huagongshe.com/reaction/1917159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-(Pyrrolidin-1-yl)ethyl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-7-amineHCID 59144163—
ReactantMethyl thiophene-2-carbimidothioate hydroiodideHCID 66704664—
SolventEthanolHCID 702—
ProductHCID 178511900HCID 17851190088%

Reaction Steps

Methyl thiophene-2-carbimidothioate hydroiodide (1.239 g, 4.34 mmol) was added to a mixture of 4-(2-(pyrrolidin-1-yl)ethyl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-7-amine (0.572 g, 2.172 mmol) in EtOH (20 mL). The reaction was stirred overnight at room temperature. The reaction was quenched with saturated sodium bicarbonate solution (30 mL). The mixture was then extracted with CH2Cl2 (50 mL), and the aqueous phase was washed with CH2Cl2 (50 mL). The combined organic fractions were washed with brine (50 mL) and dried (Na2SO4). The crude material was subject to flash chromatography on silica gel (CH2Cl2 then 5% (2M NH3MeOH)/CH2Cl2). The collected fractions gave compound 11 as light brown viscous liquid (0.71 g, 88%). 1H NMR (DMSO-d6) δ 7.69 (d, J=3.6 Hz, 1H), 7.56 (d, J=5.1 Hz, 1H), 7.08-7.06 (m, 1H), 6.67 (t, J=8.7 Hz, 1H), 6.50 (d, J=8.4 Hz, 1H), 6.46 (s, 1H), 6.32 (brs, 2H), 3.57-3.53 (m, 2H), 3.39-3.34 (m, 2H), 3.03-3.00 (m, 2H), 2.60 (t, J=7.2 Hz, 2H), 2.50 (brs, 4H), 1.68 (brs, 4H); ESI-MS (m/z, %): 375, 373 (MH+, 47), 278, 276 (100), 98 (21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618286B2
Source datasetuspto-grants-2013_12
ORD IDord-7718b4ad0765434699d43e31bb8b1ef3
Source noteuspto-grants-2013_12