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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394853Generated: November 3, 2026

HCID 11995325, compound → 13-Cyclohexyl-6,7-dihydro-5H-indolo[1,2-d][1,4]benzodiazepine-10-carboxylic acid

https://huagongshe.com/reaction/1394853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11995325HCID 11995325—
SolventSodium HydroxideHCID 14798—
SolventMeOH tetrahydrofuranHCID 21899815—
Product13-Cyclohexyl-6,7-dihydro-5H-indolo[1,2-d][1,4]benzodiazepine-10-carboxylic acidHCID 1199512476.7%

Reaction Steps

A solution of methyl 13-cyclohexyl-6,7-dihydro-5H-indolo[1,2-d][1,4]benzodiazepin-10-carboxylate (45.8 mg, 0.12 mmol) in THF/MeOH (1:2, 3 mL) and 1N aqueous NaOH (0.5 mL) was heated at 50° C. for 5 h. The reaction solution was concentrated to remove volatile organics, neutralized with TFA (0.04 mL) and purified by preparative HPLC (MeOH/H2O with TFA buffer) to yield 13-cyclohexyl-6,7-dihydro-5H-indolo[1,2-d][1,4]benzodiazepin-10-carboxylic acid (33 mg, 0.092 mmol, 76%) as white solid. 1HNMR (500 MHz, MeOD) δ 8.25 (s, 1H), 7.96 (d, J=8.5 Hz, 1H), 7.79 (dd, J=8.5, 1.2 Hz, 1H), 7.63-7.52 (m, 3H), 7.50-7.46 (m, 1H), 4.44 (br s, 2H), 3.92-3.86 (m, 2H), 3.03 (tt, J=12.4, 3.1 Hz, 1H), 2.21-2.10 (m, 2H), 1.97-1.80 (m, 5H), 1.54-1.36 (m, 2H). LCMS: m/e 361 (M+H)+, ret time 1.88 min, column C, 2 minute gradient, start at 0% B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348425B2
Source datasetuspto-grants-2008_03
ORD IDord-049fbe3f0cc44d129453cb24bc484160
Source noteuspto-grants-2008_03