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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283602Generated: November 2, 2026

2-azido-N-phenylacetamide → HCID 178508397, compound

https://huagongshe.com/reaction/2283602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-azido-N-phenylacetamideHCID 14201101—
Reactant2-Amino-4-hept-6-ynyl-imidazole-1-carboxylic acid tert-butyl esterHCID 53359534—
ProductHCID 178508397HCID 17850839752.4%

Reaction Steps

Following the general procedure, 2-amino-4-hept-6-ynyl-imidazole-1-carboxylic acid tert-butyl ester (0.075 g, 0.270 mmol) was reacted with 2-azido-N-phenyl-acetamide (0.072 g, 0.410 mmol) and afforded 0.050 g (51% yield) of 2-{4-[5-(2-amino-1H-imidazol-4-yl)-pentyl]-[1,2,3]triazol-1-yl}-N-phenyl-acetamide hydrchloride. 1H NMR (400 MHz, CD3OD) 8.53 (s, 1H), 7.59 (d, J=7.6, 2H), 7.31 (t, J=7.2, 2H), 7.11 (t, J=7.2, 1H), 6.50 (s, 1H), 5.62 (s, 2H), 3.96 (s, 1H), 2.89 (bs, 2H), 2.50 (t, J=6.8, 2H), 1.79 (bs, 2H), 1.66 (bs, 2H), 1.45 (bs, 2H); 13C NMR (100 MHz, CD3OD) δ 164.3, 148.6, 139.2, 130.1, 128.9, 125.9, 121.2, 109.8, 55.7, 28.9, 25.3, 24.7; HRMS (ESI), calculated for C18H23N7O (MH+) 353.1964. Found 353.1968.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145395B2
Source datasetuspto-grants-2015_09
ORD IDord-096ea8d59f6f4d5e870f436c03689aa9
Source noteuspto-grants-2015_09