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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949094Generated: October 31, 2026

Indole → HCID 59238883, compound

https://huagongshe.com/reaction/1949094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactanttert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylateHCID 854055—
ReactantHCID 67211699HCID 67211699—
ProductHCID 59238883HCID 59238883—

Reaction Steps

The title compound was prepared in a manner analogous to Example 28 except the starting indole is 5,7-diBOC-2,10-dichloro-6-hydroxyindolo[2,3-b]carbazole and the reagent is (S)-tert-butyl 3-hydroxypyrrolidine-1-carboxylate. 1H-NMR (400 MHz, CDCl3) δ ppm 9.27 (br s, 2 H), 8.35 (s, 1 H), 8.07 (s, 2 H), 7.38-7.30 (m, 4 H), 5.09 (t, J=4.0 Hz, 1 H), 3.55-3.46 (m, 2 H), 3.29 (d, J=12.0 Hz, 1 H), 3.15 (td, J=10.0, 4.8 Hz, 1 H), 2.83 (dd, J=11.6, 3.6 Hz, 1 H), 2.38-2.28 (m, 1 H), 2.21-2.10 (m, 1 H); MS (ESI) m/z 408.2 (M−H)−; MS (ESI) m/z 410.1 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399502B2
Source datasetuspto-grants-2013_03
ORD IDord-aa4a09a077d94832bec1dee701fa0419
Source noteuspto-grants-2013_03