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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28697Generated: October 25, 2026

2-Chlorobenzoyl chloride → N-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-2-chlorobenzamide

https://huagongshe.com/reaction/28697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl chlorideHCID 69110—
Reactant6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amineHCID 597879—
ProductN-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-2-chlorobenzamideHCID 11177152—

Reaction Steps

N-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-2-chlorobenzamide was prepared from 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine and 2-chlorobenzoyl chloride in a similar manner as described above to give a white solid (30% yield). 1H-NMR (DMSO-d6): δ 10.98 (s, 1H), 8.89 (d, 1H), 7.54 (dd, 2H), 7.48-7.44 (m, 1H), 7.42 (dd, 1H), 7.40-7.34 (m, 1H), 7.28 (d, 1H), 7.13 (dd, 1H), 5.26 (m, 1H), 2.60 (m, 2H), 2.08-1.91 (m, 2H), 1.90-1.73 (m, 2H); MS m/z 403 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419997B2
Source datasetuspto-grants-2008_09
ORD IDord-c2b0d821e7114280bc5caffe67be4f3c
Source noteuspto-grants-2008_09