Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907410Generated: October 31, 2026

HCID 86762147, compound → HCID 86762148, compound

https://huagongshe.com/reaction/1907410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86762147HCID 86762147—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86762148HCID 8676214894.5%

Reaction Steps

A suspension of tert-butyl ((4aR,7aR)-7a-(5-azido-2-fluorophenyl)-4a,5,6,7a-tetrahydro-4H-furo[2,3-d][1,3]thiazin-2-yl)carbamate (50 mg, 0.127 mmol), 10% Pd/C (135 mg, 0.127 mmol) in methanol (5525 μL) was stirred under hydrogen balloon at rt for 12 h. The reaction mixture was filtered and the filtrate was evaporated in vacuo to tert-butyl ((4aS,7aS)-7a-(5-amino-2-fluorophenyl)-4a,5,6,7a-tetrahydro-4H-furo[2,3-d][1,3]thiazin-2-yl)carbamate (44 mg, 0.120 mmol, 94% yield) as a yellowish oil. This material was used directly for the next reaction without purification. MS (M+H)+: 368.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598161B2
Source datasetuspto-grants-2013_12
ORD IDord-89a5113590e0473aac02489a99adca5b
Source noteuspto-grants-2013_12