Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420302Generated: October 31, 2026

5-Tert-butoxycarbonylamino-3-(3,5-difluoro-4-nitro-benzyl)-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl ester → HCID 57386307, compound

https://huagongshe.com/reaction/420302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Tert-butoxycarbonylamino-3-(3,5-difluoro-4-nitro-benzyl)-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl esterHCID 66649597—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57386307HCID 57386307—

Reaction Steps

To a degassed solution of 5-tert-butoxycarbonylamino-3-(3,5-difluoro-4-nitro-benzyl)-4-oxo-tetrahydro-thiopyran-3-carboxylic acid allyl ester (30.4 g, 62.4 mmol) in THF (300 mL) was added under argon 5,5-dimethyl-cyclohexane-1,3-dione (11.6 g, 81.2 mmol) and Pd(PPh3)4 (0.76 g, 0.62 mmol) and the reaction mixture was stirred for 3 h at 25° C. The reaction mixture was poured into aq. NaH2PO4 solution, concentrated and extracted with EtOAc. Combined organic extracts were washed with brine, dried over MgSO4, filtered and evaporated. The crystallized product containing the (3R*,5S*)-diastereoisomer was filtered off and dried. The mother liquor containing a larger amount of the (3S*,5S*)-diastereoisomer was dissolved in THF and equilibrated with a catalytic amount of DBU to the (3R*,5S*)-diastereoisomer for 16 h at 25° C. After removal of the THF the (3R*,5S*)-diastereoisomer was crystallized from Et2O-hexane to provide more of the title compound as white crystals: TLC (hexane-EtOAc 3:1) Rf=0.23; HPLC RtA=2.23 min; ESIMS [M+NH4]+=420; 1H NMR (400 MHz, CDCl3): δ 6.96 (d, 2H), 5.65 (d, 1H), 4.55 (m, 1H), 3.40 (m, 1H), 3.25 (dd, 1H), 3.14 (m, 1H), 2.86 (m, 1H), 2.6-2.75 (m, 3H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-4ae25ecadf04445b94047a3f950e690a
Source noteuspto-grants-2012_01