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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284326Generated: November 2, 2026

(1h-indol-2-ylmethyl)amine → HCID 67113397, compound

https://huagongshe.com/reaction/2284326

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1h-indol-2-ylmethyl)amineHCID 582331—
ReactantHCID 63748409HCID 63748409—
ReactantHCID 67112874HCID 67112874—
ProductHCID 67113397HCID 67113397—

Reaction Steps

Compound 963 was prepared according to the procedure described in Scheme IV from 4-(5-amino-1H-indol-1-yl)benzoic acid, 2-aminomethylindole, and 1-(2-hydroxyethyl)-1H-indole-5-carboxylic acid. 1H NMR (500 MHz, DMSO-d6) δ 10.14 (s, 1H), 9.42 (s, 1H), 8.31 (dd, J=1.0, 5.5 Hz, 2H), 8.14 (d, J=8.5 Hz, 2H), 8.06 (t, J=5.5 Hz, 1H), 7.87 (dd, J=1.5, 9 Hz, 1H), 7.74 (d, J=8 Hz, 1H), 7.66 (d, J=9 Hz, 2H), 7.62 (d, J=2 Hz, 1H), 7.61 (s, 1H), 7.57 (d, J=3 Hz, 1H), 7.55 (d, J=9 Hz, 1H), 7.37 (d, J=2.5 Hz, 1H), 7.11 (ddd, J=1, 7, 9 Hz, 1H) 7.03 (ddd, J=1, 7, 8.5 Hz, 1H), 6.70 (d, J=3.5 Hz, 1H), 6.56 (d, J=3.5 Hz, 1H), 4.82 (d, J=5.5 Hz, 2H), 4.35 (t, J=5.5 Hz, 2H), 3.92 (q, J=5 Hz, 2H), 3.31 (d, J=5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09144557B2
Source datasetuspto-grants-2015_09
ORD IDord-583c114ff5684d9aa1a7784f39947720
Source noteuspto-grants-2015_09