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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117902Generated: October 30, 2026

N,N'-Bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine → HCID 178474439, compound

https://huagongshe.com/reaction/2117902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-Bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidineHCID 4428040—
ReactantBistrimethylsilylacetamidHCID 11708267—
Reactant2-(Acetylamino)-4-[2-(4-aminophenyl)ethyl]-1,3-thiazole-5-carboxylic acidHCID 21915248—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178474439HCID 17847443960.9%

Reaction Steps

2-(Acetylamino)-4-[2-(4-aminophenyl)ethyl]-1,3-thiazole-5-carboxylic acid (106 mg) was suspended in THF (2 ml) under N2 atmosphere. Bis(trimethylsilyl)acetamide (0.253 ml) was added to the suspension at r.t., and the mixture was stirred at r.t. for 15 minutes. Then, N,N′-bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine (119 mg) was added to the solution at r.t. The reaction mixture was stirred at r.t. for 20 hours, and concentrated in vacuo. The residue was dissolved in CHCl3. The organic solution was washed with 1N—HCl, water and brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residual solid was washed with ethyl ether to give 2-(acetylamino)-4-{2-[4-({(Z)-[(tert-butoxycarbonyl)amino](tert-butoxycarbonyl)iminomethyl}amino)phenyl]ethyl}-1,3-thiazole-5-carboxylic acid (115.8 mg) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-fcc28ac99d3e42a09d16e8482d9ff396
Source noteuspto-grants-2008_10