Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590760Generated: October 30, 2026

benzyl (1S,3S,4S)-3-acetamido-3-(tert-butylcarbamoyl)-4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)cyclopentylcarbamate → HCID 69669595, compound

https://huagongshe.com/reaction/590760

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl (1S,3S,4S)-3-acetamido-3-(tert-butylcarbamoyl)-4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)cyclopentylcarbamateHCID 86665798—
CatalystPalladium hydroxideHCID 9942167—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 69669595HCID 69669595100%

Reaction Steps

While under nitrogen, a stirred solution of benzyl (1S,3S,4S)-3-acetamido-3-(tert-butylcarbamoyl)-4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)cyclopentylcarbamate (0.544 g, 1.00 mmol) in 4:1 ethyl acetate/methanol (20 mL) was treated with 20% Pd(OH)2/C (0.30 g), purged with hydrogen, and stirred under a balloon for 18 h. The mixture was purged with nitrogen and carefully filtered through a pad of Celite® (without letting filter pad dry) and the filtrate concentrated in vacuo to afford 0.409 g (100%) of the subject compound as a white solid. NMR (CDCl3): δ 6.72 (br s, 1 H), 6.67 (br s, 1 H), 3.63 (m, 1 H), 2.80 (m, 1 H), 2.57 (m, 1 H), 1.75-2.00 (m, 4 H), 1.93 (s, 3 H), 1.00-1.50 (m, 3 H), 1.25 (s, 9 H), 1.17 (s, 12 H), 0.60-0.75 (m, 2 H). MS (M+1): 410.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233985B2
Source datasetuspto-grants-2016_01
ORD IDord-891f00ed5c8a4959aedbc21e8a45f6eb
Source noteuspto-grants-2016_01