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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077601Generated: October 26, 2026

Cyclohexanecarboxylic acid → N-(6-bromobenzo[d]thiazol-2-yl)cyclohexanecarboxamide

https://huagongshe.com/reaction/2077601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxylic acidHCID 7413—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Benzothiazolamine, 6-bromo-HCID 85149—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDichloromethaneHCID 6344—
ProductN-(6-bromobenzo[d]thiazol-2-yl)cyclohexanecarboxamideHCID 460461578.4%

Reaction Steps

A mixture of Hunig's base (286 μl, 1637 μmol), HATU (830 mg, 2182 μmol) and cyclohexanecarboxylic acid (147 mg, 1146 μmol) was dissolved in 2.0 mL CH2Cl2 and stirred at room temperature for 10 min. 6-bromobenzo[d]thiazol-2-amine (250 mg, 1091 μmol) was added, and stirring was continued overnight. The solids were filtered and washed with CH2Cl2. The filtrate was concentrated, dissolved in CH2Cl2 and purified by silica gel chromatography using 100% CH2Cl2 to provide N-(6-bromobenzo[d]thiazol-2-yl)cyclohexanecarboxamide (290 mg, 78% yield) as a white solid. MS (ESI pos. ion) m/z calc'd for C14H15BrN2OS: 339.3/341.3. found 339.0/341.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928140B2
Source datasetuspto-grants-2011_04
ORD IDord-9ed56c1abbf44a52bf197a3bc1952a2c
Source noteuspto-grants-2011_04