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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111443Generated: November 2, 2026

2486-69-3 → HCID 68737897, compound

https://huagongshe.com/reaction/2111443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2486-69-3HCID 288057—
ReactantHCID 86623424HCID 86623424—
SolventEthanol water hydrochloric acidHCID 86604601—
ProductHCID 68737897HCID 68737897—

Reaction Steps

A mixture of 0.15 g (0.0006 mole) of (R)-9-chloro-6-methyl-2,3,3a,4-tetrahydro-1H,6H-6,8,10,10b-tetraaza-benzo[e]azulen-5-one (VII-102) and 0.11 g (0.00066 mole) of 4-amino-3-methoxy-benzoic acid (Aldrich) in 15 mL of ethanol-water-hydrochloric acid (20:80:1) was heated by microwave at 160 degrees for 40 minutes, and then concentrated under reduced pressure. The residue was lyophilized to give crude 3-methoxy-4-((R)-6-methyl-5-oxo-2,3,3a,4,5,6-hexahydro-1H-6,8,10,10b-tetraaza-benzo[e]azulen-9-ylamino)-benzoic acid (I-102a) as a light yellow solid which was used without further purification in subsequent steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517873B2
Source datasetuspto-grants-2009_04
ORD IDord-09dd87e3c69a4a568a36813b20bdcca7
Source noteuspto-grants-2009_04