Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895558Generated: November 4, 2026

HCID 66887685, compound → HCID 49854434, compound

https://huagongshe.com/reaction/1895558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66887685HCID 66887685—
SolventAcetic AcidHCID 176—
ProductHCID 49854434HCID 49854434—

Reaction Steps

Step-3: A solution of tert-butyl 3-((2-amino-3-carbamoylphenyl)carbamoyl)-7-((tert-butoxycarbonyl)amino)-3,4-dihydroisoquinoline-2(1H)-carboxylate (70 mg, 0.133 mmol) in acetic acid (2 ml) was heated to 80° C. and stirred for 2.5 h. The reaction mixture was concentrated, neutralized with aq. NaHCO3 and extracted with DCM. The DCM layer was washed with brine, dried over anhydrous sodium sulfate and evaporated. Purification of the crude product by preparative TLC using methanol/dichloromethane (1:15) mixture as eluent afforded tert-butyl 7-((tert-butoxycarbonyl)amino)-3-(4-carbamoyl-1H-benzo[d]imidazol-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate. MS (ES+): m/z 508.28 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513433B2
Source datasetuspto-grants-2013_08
ORD IDord-0727199c5aaf4fee9d4f2e2bd64a6369
Source noteuspto-grants-2013_08