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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339241Generated: October 29, 2026

(S)-tert-butyl 7-nitro-3-(((R)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate → (S)-tert-Butyl 7-amino-3-(((R)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

https://huagongshe.com/reaction/339241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-butyl 7-nitro-3-(((R)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 86705876—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(S)-tert-Butyl 7-amino-3-(((R)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 8670587584%

Reaction Steps

To a pressure flask containing 5% Pd/C (91 mg, 0.085 mg) was added a solution of (S)-tert-butyl 7-nitro-3-(((R)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (0.38 g, 0.85 mmol) in MeOH (8.5 mL). The resulting reaction mixture was stirred under 5 psi H2 for 1 h and then filtered through a pad of CELITE®, rinsing with EtOAc. The filtrate was concentrated in vacuo to give the title compound (301 mg, 84%) as a colorless oil. MS (ESI+) m/z 422.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889712B2
Source datasetuspto-grants-2014_11
ORD IDord-bacec420aa1a4b84b90d6b6bb1194104
Source noteuspto-grants-2014_11