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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297837Generated: November 2, 2026

5-Amino-2-methylindole → HCID 18382880, compound

https://huagongshe.com/reaction/2297837

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-methylindoleHCID 2733992—
ReactantHCID 18382780HCID 18382780—
ProductHCID 18382880HCID 18382880—

Reaction Steps

The title compound was prepared from 2-methyl-5-aminoindole and 2-(7-chloro-thieno[3,2-b]pyridin-2-yl)-benzooxazole by the procedure analogous to example 148(c) above. 1H NMR (400 MHz, CD3OD) δ8.18 (d, 1H), 8.10 (s, 1H), 7.70 (m, 2H), 7.40 (m, 4H), 6.98 (d, 1H), 6.68 (d, 1H), 6.14 (s, 1H), 2.43 (s, 3H); RP18-HPLC RT: 6.13 minutes; API MS 397 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492383B1
Source datasetuspto-grants-2002_12
ORD IDord-7cee45a7522648b2a40cfc5cd70ee071
Source noteuspto-grants-2002_12