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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988458Generated: October 25, 2026

Boron tribromide → 2-(Cyclohexylmethylamino)benzo[d]thiazol-6-ol

https://huagongshe.com/reaction/1988458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantN-(cyclohexylmethyl)-6-methoxy-1,3-benzothiazol-2-amineHCID 57725688—
SolventDichloromethaneHCID 6344—
Product2-(Cyclohexylmethylamino)benzo[d]thiazol-6-olHCID 5772554099.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of N-(cyclohexylmethyl)-6-methoxybenzo[d]thiazol-2-amine (1.40 g, 5.05 mmol) in 12 ml of DCM was added 1 M boron tribromide in DCM (10.6 ml, 10.6 mmol) slowly over about 3 minutes at 0° C. The reaction solution was stirred at 0° C. for 20 min and then at RT. for 2 hr. The reaction mixture was concentrated to a solid. To the residual solids add 200 ml of ethyl acetate and 50 ml of water and stir at RT. for 10 minutes. With stirring, carefully add excess solid NaHCO3 until basic. Stir at RT. about 1 hour to dissolve the solids. Remove the aqueous layer and extract with 100 ml of ethyl acetate. Combine organic layers and wash with 1×30 ml water, 1×25 ml saturated NaCl solution and dry with sodium sulfate. This mixture was filter through a silica gel plug (1.25 in.×3 in.) and flushed with ethyl acetate. The filtrate was concentrated under reduced pressure to give 2-(cyclohexylmethylamino)benzo[d]thiazol-6-ol as solid (1.32 grams). ES/MS m/z 263.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553854B2
Source datasetuspto-grants-2009_06
ORD IDord-079d5a009eb34ff78e68208485a113cd
Source noteuspto-grants-2009_06