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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582455Generated: November 1, 2026

Methanol → HCID 9901146, compound

https://huagongshe.com/reaction/1582455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium formateHCID 2723923—
ReactantHCID 10222398HCID 10222398—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
ProductHCID 9901146HCID 990114697.5%

Reaction Steps

(Chart D, Step 4): A dry round bottom flask is charged with 3-benzyl-11-(2-phenoxyethyl)-2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,7-a]indole (317 mg, 0.80 mmol), ammonium formate (254 mg, 4.0 mmol), methanol (18 mL) and dichloromethane (3.2 mL). After the addition of 10% Pd/C (64 mg) the reaction is stirred at ambient temperature for two days. The reaction mixture is filtered through a pad of celite, and the catalyst is rinsed with methanol. The filtrates are combined and concentrated to 380 mg of a crude solid. This material is recrystallized from ethyl acetate/methanol/ethyl ether to afford 239 mg of 11-(2-phenoxyethyl)-2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,7-a]indole as a white solid. IR (drift) 3026, 3015, 2998, 2983, 2948, 2910, 2869, 2806, 2781, 2752, 1468, 1451, 1245, 755, 746 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734301B2
Source datasetuspto-grants-2004_05
ORD IDord-6f9f989825fb4594a144f685f604e870
Source noteuspto-grants-2004_05