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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518304Generated: November 4, 2026

tert-butyl 2-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-5-(3-hydroxyprop-1-ynyl)thiazole-4-carboxylate → tert-butyl 2-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-5-(3-hydroxypropyl)thiazole-4-carboxylate

https://huagongshe.com/reaction/1518304

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 2-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-5-(3-hydroxyprop-1-ynyl)thiazole-4-carboxylateHCID 59447612—
CatalystAdams' catalystHCID 345198—
SolventEthyl AcetateHCID 8857—
Producttert-butyl 2-(8-(benzo[d]thiazol-2-yl((2-(trimethylsilyl)ethoxy)methyl)carbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-5-(3-hydroxypropyl)thiazole-4-carboxylateHCID 59447663—

Reaction Steps

To a solution of methyl 2-(8-(benzo[d]thiazol-2-ylcarbamoyl)-3,4-dihydroisoquinolin-2(1H)-yl)-5-(3-hydroxyprop-1-ynyl)thiazole-4-carboxylate (38D) (2.0 g, 3.96 mmol) in EtOAc (20 mL) was added PtO2 (240 mg, 1.1 mmol). The mixture was stirred at rt under hydrogen (balloon) overnight. The mixture was then filtered and the filtrate was concentrated under reduced pressure to provide the desired product 38E: 1H NMR (300 MHz, CDCl3) δ ppm 8.30 (1H, m), 7.71 (1H, d), 7.59 (1H, m), 7.49 (1H, m), 7.35 (3H, m), 6.00 (2H, s), 5.14 (2H, s), 3.95 (2H, m), 3.75 (2H, t), 3.63 (2H, m), 3.17 (2H, t), 3.07 (2H, t), 2.40 (1H, t), 1.89 (2H, m), 1.58 (9H, d), 0.98 (2H, t), 0.01 (9H, m). MS (ESI(+)): m/z 681 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232273B2
Source datasetuspto-grants-2012_07
ORD IDord-b044092ad0c74968aa04df6c3ee590f6
Source noteuspto-grants-2012_07