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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167283Generated: November 2, 2026

HCID 480312, compound → HCID 480397, compound

https://huagongshe.com/reaction/1167283

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 (s, 3H), 2.57-2.10 (br, 2H), 1.82-1.07 (m, 6H), 1.04 (s, H), 0.92 (s, 3H). MS(ESI): 619(M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617350B2
Source datasetuspto-grants-2003_09
ORD IDord-cf298f9bc621426a99f6376f02bfa9b0
Source noteuspto-grants-2003_09