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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470663Generated: October 30, 2026

(3'S,4'R,7'S,8'S,8a'R)-6''-chloro-8'-(3-chloro-2-fluorophenyl)-4,4-dimethyl-3',4'-diphenyl-3',4',8',8a'-tetrahydro-1'H-dispiro[cyclohexane-1,6'-pyrrolo[2,1-c][1,4]oxazine-7',3''-pyrrolo[2,3-b]pyridine]-1',2''(1''H)-dione → HCID 178423624, compound

https://huagongshe.com/reaction/470663

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3'S,4'R,7'S,8'S,8a'R)-6''-chloro-8'-(3-chloro-2-fluorophenyl)-4,4-dimethyl-3',4'-diphenyl-3',4',8',8a'-tetrahydro-1'H-dispiro[cyclohexane-1,6'-pyrrolo[2,1-c][1,4]oxazine-7',3''-pyrrolo[2,3-b]pyridine]-1',2''(1''H)-dioneHCID 86672583—
ReactantHCID 178511560HCID 178511560—
ProductHCID 178423624HCID 17842362483.4%

Reaction Steps

The compound (260 mg, 0.39 mmol) obtained in Step 1 above and (trans-4-aminocyclohexyl)methanol (100 mg, 0.77 mmol) were used as starting materials and treated in the same way as in Step 2 of Example 1 to give 260 mg (83%) of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629133B2
Source datasetuspto-grants-2014_01
ORD IDord-af662f47bb524c0c88ee85523a849c1d
Source noteuspto-grants-2014_01