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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28712Generated: October 30, 2026

6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amine → N-(6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-1H-imidazole-4-carboxamide

https://huagongshe.com/reaction/28712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amineHCID 17743497—
ReactantHCID 178524800HCID 178524800—
ProductN-(6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-1H-imidazole-4-carboxamideHCID 178521857—

Reaction Steps

N-(6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-1H-imidazole-4-carboxamide was prepared from 4-imidazole carboxylic acid and 6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amine in a similar manner as described above to give a white solid (4% yield). 1H-NMR (CDCl3): δ 9.19 (s, 1H), 7.62 (s, 1H), 7.57 (s, 1H), 7.41 (s, 1H), 7.37 (d, 1H), 7.17 (d, 1H), 7.05 (dd, 1H), 6.60 (d, 1H), 5.25 (m, 1H), 2.62 (m, 2H), 2.21 (m, 1H), 1.91 (m, 3H); MS m/z 313 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419997B2
Source datasetuspto-grants-2008_09
ORD IDord-98fa6796a8f14b7fa694ff5979cb375b
Source noteuspto-grants-2008_09