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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117722Generated: October 31, 2026

HCID 480312, compound → HCID 480397, compound

https://huagongshe.com/reaction/2117722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 480312HCID 480312—
CatalystNickelHCID 935—
SolventAmmonia methanolHCID 21705897—
ProductHCID 480397HCID 48039777.3%

Reaction Steps

A mixture of 0.29 g (0.46 mmol) of (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-[(1S,2R)-1-benzyl-3-((4-cyano-2,2-dimethylbutyl)[3-(methylamino)phenyl]sulfonylamino)-2-hydroxypropyl]carbamate and approximately 50 mg of Raney nickel (washed with water and MeOH) in 60 mL of 2M NH3/MeOH was subjected to hydrogenation at 45 psi. After 1.5 hours the reaction vessel was purged with nitrogen, catalyst removed by filtration through celite and the filtrate concentrated in vacuo. The residue was subjected to flash chromatography (SiO2, 9:1 CH2Cl2/2M NH3 in MEOH) to afford 0.22 g (76%) of the desired amine as a white foam. NMR (CDCl3): 7.39-7.19 (m, 6H), 7.10 (d, 1H), 7.04-6.92 (m, 2H), 6.81 (dd, 1H), 5.63 (d, 1H), 5.05 (q, 1H), 4.16 (br s, 1H), 4.09-3.80 (m, 4H), 3.70 (m, 2H), 3.31 (m, 2H), 3.21-3.00 (m, 3H), 2.99-2.58 (m, 5H), 2.90 (3, 3H), 2.57-2.10 (br, 2H), 1.82-1.07 (m, 6H), 1.04 (s, 3H), 0.92 (s, 3H). MS(ESI): 619 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442718B2
Source datasetuspto-grants-2008_10
ORD IDord-b46cc3da72a746379a0fefded11ddd97
Source noteuspto-grants-2008_10