Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223084Generated: November 1, 2026

HCID 59713676, compound → HCID 10196661, compound

https://huagongshe.com/reaction/2223084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59713676HCID 59713676—
ReactantHCID 59713770HCID 59713770—
ProductHCID 10196661HCID 1019666156%

Reaction Steps

A solution of 7-chloro-1,3-dihydro-3-isothiocyanato-1-methyl-5-(3-pyridinyl)-2H-1,4-benzodiazepin-2-one (0.0282 g, 0.0823 mmol) and 4-(4-morpholinyl)-1-naphthalenamine (0.0188 g, 0.0823 mmol) in (CH2Cl)2 (2.5 mL) was heated at 70° C. for 24 h. The reaction was cooled and concentrated in vacuo, and the residue was purified by silica gel column chromatography (1:2 CH2Cl2:EtOAc) to provide the title compound (0.0263 g, 56%). 1H-NMR (CDCl3): δ 8.72-8.68 (m, 2H), 8.29-8.25 (m, 1H), 8.11-8.07 (m, 1H), 8.05-8.00 (m, 2H), 7.64-7.55 (m, 5H), 7.38-7.33 (m, 3H), 7.15 (d, J=8.0 Hz, 1H), 6.08 (d, J=7.6 Hz, 1H), 4.03-3.96 (br m, 4H), 3.39 (s, 3H), 3.15 (br s, 4H). HRMS calculated for (C30H27ClN6O2S+H) (M+H)+: 571.1683. Found (ESI): 571.1699. Anal. Calcd for C30H27ClN6O2S+0.7 H2O: C, 61.73; H, 4.90; N, 14.40. Found: C, 61.93;H, 4.79; N, 13.87.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375101B2
Source datasetuspto-grants-2008_05
ORD IDord-0db27936fc304f869c377975cec71592
Source noteuspto-grants-2008_05