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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040958Generated: November 2, 2026

Water → (S)-1-(6-iodobenzo[d]thiazol-2-yl)pyrrolidin-3-ol

https://huagongshe.com/reaction/2040958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(3S)-pyrrolidin-3-olHCID 2733874—
Reactant6-Iodo-2-(methylsulfonyl)benzo[d]thiazoleHCID 66906139—
SolventDimethylformamideHCID 6228—
Product(S)-1-(6-iodobenzo[d]thiazol-2-yl)pyrrolidin-3-olHCID 66905790—

Reaction Conditions

Temperature150 °C

Reaction Steps

A stirred mixture of 6-iodo-2-(methylsulfonyl)benzo[d]thiazole (Reference Example 6c, 1.50 g, 4.42 mmol), (S)-pyrrolidin-3-ol (0.500 g, 5.74 mmol), and potassium carbonate (1.222 g, 8.84 mmol) in N,N-dimethylformamide (21.5 mL) was heated to 150° C. under microwave irradiation for 10 minutes. The reaction mixture was cooled to room temperature, then poured into water (350 mL) to give a precipitate. The precipitate was collected by filtration, rinsed with water, and then dissolved in ethyl acetate. The ethyl acetate solution was dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure to give a crude solid that was purified by silica gel chromatography (100% CHCl3 to 97:3 CHCl3/methanol). Fractions containing product were combined an concentrated under reduced pressure to provide (S)-1-(6-iodobenzo[d]thiazol-2-yl)pyrrolidin-3-ol. 1H NMR (300 MHz, CD3OD) δ ppm 2.03-2.14 (m, 1H), 2.15-2.29 (m, 1H), 3.47-3.55 (m, 1H), 3.58-3.75 (m, 3H), 4.53-4.59 (m, 1H), 7.23 (d, J=8 Hz, 1H), 7.53-7.59 (m, 1H), 7.95-7.98 (m, 1H); MS (DCI/NH3) m/z 347 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580968B2
Source datasetuspto-grants-2013_11
ORD IDord-ab0797c16f3145c5bf68283efdd06899
Source noteuspto-grants-2013_11