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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749759Generated: October 30, 2026

4-Nitrobenzyl bromide → HCID 11773499, compound

https://huagongshe.com/reaction/749759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl bromideHCID 66011—
Reactant3-(4-chloro-phenyl)-4,5,7,8-tetrahydro-1H-1,2,6-triaza-azulene-6-carboxylic acid tert-butyl esterHCID 67269020—
ProductHCID 11773499HCID 117734991.2%

Reaction Steps

The title compound (0.004 g) was prepared from 3-(4-chloro-phenyl)-4,5,7,8-tetrahydro-1H-1,2,6-triaza-azulene-6-carboxylic acid tert-butyl ester (Example 59, Step C; 0.3 g) using 4-nitrobenzyl bromide (0.3 g) in place of benzyl chloride. MS (ESI): exact mass calculated for C20H19ClN4O2, 382.12; found, m/z 383.1 [M+H]+. 1H NMR (400 MHz, CD3OD): 8.23-8.19 (m, 2H), 7.51-7.47 (m, 2H), 7.45-7.47 (m, 2H), 7.32 (d, J=8.6 Hz, 2H), 5.52 (s, 2H), 2.98-2.95 (m, 4H), 2.89-2.85 (m, 2H), 2.83-2.79 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402680B2
Source datasetuspto-grants-2008_07
ORD IDord-c086e6cffa6a4ad7bacd12a885d5d148
Source noteuspto-grants-2008_07