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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236111Generated: October 31, 2026

Hydrochloric Acid → HCID 86614346, compound

https://huagongshe.com/reaction/2236111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenyl isocyanateHCID 7672—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl (1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetate hydrochlorideHCID 71552668—
SolventDichloromethaneHCID 6344—
ProductHCID 86614346HCID 86614346—

Reaction Steps

Step a): To a stirred solution of Intermediate 1 (20 mg, 0.068 mnol) and DIEA (35 μl, 0.20 mmol) in dichloromethane (1 ml) is added phenyl isocyanate (8.2 μl, 0.075 mmol). The reaction mixture is kept stirring at rt for 1 h, then 1N HCl (2 ml) was added. The aqueous layer is extracted twice with dichloromethane. The organic layers are combined and the solvent is evaporated to give crude ethyl (2-phenylcarbamoyl-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetic acid: tR (LC-2) 2.23 min; ESI-MS (positive ion): m/z 400.39 [M+Na]+ (calcd 377.44 for C22H23N3O3); 1H-NMR (CDCl3): 1.19 (t, J=7.0 Hz, 3H); 2.77 (t, J=5.3 Hz, 2H); 3.91 (t, J=5.3 Hz, 2H); 4.14 (q, J=7.0 Hz, 2H); 4.65 (s, 2H); 4.68 (s, 2H); 6.46 (s, 1H); 6.98 (t, J=7.0 Hz, 1H); 7.04-7.09 (m, 1H); 7.14-7.16 (m, 2H); 7.20-7.26 (m, 2H); 7.32-7.35 (m, 2H); 7.40 (d, J=7.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714132B2
Source datasetuspto-grants-2010_05
ORD IDord-1526a124ecdd4467a7df569bf1e5f46c
Source noteuspto-grants-2010_05