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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592356Generated: November 1, 2026

phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate → HCID 44447136, compound

https://huagongshe.com/reaction/1592356

Reaction equation

Participants

RoleNameHCIDCharge
Reactantphenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamateHCID 22252681—
ReactantHCID 58997665HCID 58997665—
SolventAcetonitrileHCID 6342—
ProductHCID 44447136HCID 4444713678.5%

Reaction Steps

The product of Step g (50 mg, 0.19 mmol, 1 eq.), phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate (55 mg, 0.19 mmol, 1 eq.) and acetonitrile (3 mL) were mixed at 25° C. under N2 overnight. Worked up by stripping off the solvents then purifying the residue over silica gel in 100% EtOAc to 4:1 EtOAc/MeOH. Obtained 70 mg of a white glass as product. NMR (300 MHz, CDCl3) δ 7.86 (s, 1H); 7.6 (d, 1H, J=7 Hz); 7.38 (t, 1H, J=7 Hz); 7.29 (d, 1H, J=7 Hz); 7.20-7.00 (m, 2H); 6.92 (t, 2H, J=7 Hz); 4.13 (s, 3H) 4.05-3.85 (m, 1H); 3.80-3.60(m, 1H); 2.80-2.40 (m, 8H); 1.85-1.60 (m, 2H); 1.18 (d, 3H, J=7 Hz); 1.00 (t, 3H, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291744B2
Source datasetuspto-grants-2007_11
ORD IDord-a8e37679b068426dae28dab54e27d5e0
Source noteuspto-grants-2007_11