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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571357Generated: November 1, 2026

Sodium triacetoxyborohydride → (3aR,5R,6aR)-5-(((3S*,4S*)-3-Methoxytetrahydro-2H-pyran-4-yl)amino)-3a-(7-(trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)hexahydrocyclopenta-[c]pyrrole-2(1H)-carboxamide

https://huagongshe.com/reaction/571357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Methoxyoxan-4-oneHCID 23533610—
Reactant(3aR,5R,6aR)-5-Amino-3a-(7-(trifluoromethyl)-1,2,3,4-tetrahydro-isoquinoline-2-carbonyl)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxamideHCID 86708901—
SolventDichloromethaneHCID 6344—
Product(3aR,5R,6aR)-5-(((3S*,4S*)-3-Methoxytetrahydro-2H-pyran-4-yl)amino)-3a-(7-(trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)hexahydrocyclopenta-[c]pyrrole-2(1H)-carboxamideHCID 86708904—

Reaction Steps

A mixture of the product from Step B (316 mg, 0.62 mmol), 3-methoxydihydro-2H-pyran-4(3H)-one (242 mg, 1.86 mmol), 4 Å molecular sieves (0.3 g) and TEA (0.259 mL, 1.86 mmol) in DCM (8 mL) was stirred at rt for 2 h, followed by addition of sodium triacetoxyborohydride (263 mg, 1.24 mmol). The resulting mixture was stirred at rt overnight. The reaction was quenched by the addition of saturated NaHCO3 aqueous solution, extracted with DCM, and dried over Na2SO4. After removal of the solvent, the residue was purified by column chromatography (eluent: EtOAc to 15% 7N NH3 in methanol in EtOAc) to give the product as a white foam. 1H-NMR (400 MHz, CDCl3): δ 1.76 (br. s., 1H), 1.89-2.41 (m, 4H), 2.53 (br. s., 1H), 2.85-2.99 (m, 2H), 3.06-4.02 (m, 18H), 4.12 (q, J=7.1 Hz, 1H), 4.69 (br. s., 2H), 5.17-5.31 (m, 1H), 7.25 (d, J=7.8 Hz, 1H), 7.34-7.49 (m, 2H); LC/MS: C25H33F3N4O4: m/z 511.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024017B2
Source datasetuspto-grants-2015_05
ORD IDord-fa53d4cb156745c7bc717405fb31db8e
Source noteuspto-grants-2015_05