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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254488Generated: November 3, 2026

Potassium Carbonate → (S)-tert-butyl 4-((1,1-diethoxypropan-2-ylamino)methyl)benzo[d]thiazol-2-ylcarbamate

https://huagongshe.com/reaction/1254488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2S)-1,1-Diethoxy-2-propanamineHCID 12398111—
Reactant4-Bromomethyl-2-bis(tert-butoxycarbonyl)aminobenzothiazoleHCID 67075205—
SolventAcetonitrileHCID 6342—
Product(S)-tert-butyl 4-((1,1-diethoxypropan-2-ylamino)methyl)benzo[d]thiazol-2-ylcarbamateHCID 86652568140.8%

Reaction Conditions

Temperature65 °C

Reaction Steps

To the solution of (S)-1,1-diethoxypropan-2-amine (Compound XIX-1) 442 mg (3.00 mmol) in acetonitrile 5 ml, 4-bromomethyl-2-bis(tert-butoxycarbonyl)aminobenzothiazole (Compound XXI-1) 133 mg (0.30 mmol) and potassium carbonate 62 mg (0.45 mmol) were added and stirred at 65° C. for 2 hours. The reaction mixture was concentrated in vacuo and the residue was diluted with ethyl acetate 100 ml and washed with water 100 ml and brine 100 ml. The organic phase was dried with magnesium sulfate 1 g and filtered. The filtrate was concentrated in vacuo and the residue was purified on silica gel column chromatography (chloroform:methanol=100:0 to 95:5) to obtain the title compound 173 mg (yield 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455488B2
Source datasetuspto-grants-2013_06
ORD IDord-b42cde7da68d4b70b264fcd25bba3f1f
Source noteuspto-grants-2013_06