Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748855Generated: October 30, 2026

HCID 178502362, compound → HCID 178502362, compound

https://huagongshe.com/reaction/1748855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178502362HCID 178502362—
ReactantHCID 178502367HCID 178502367—
ProductAmmonium AcetateHCID 517165—
ProductHCID 178502362HCID 17850236287%
ProductHCID 178502367HCID 178502367—

Reaction Steps

Phenylmethyl (8S)-8-(4-{4′-[2-((2S)-1-{N-[(methyloxy)carbonyl]-L-valyl}-2-pyrrolidinyl)-1H-imidazol-4-yl]-4-biphenylyl}-1H-imidazol-2-yl)-1,4-dithia-7-azaspiro[4.4]nonane-7-carboxylate (Intermediate 38) (497 mg, 87%) was obtained from phenylmethyl (8S)-8-({[2-(4′-{2-[(2S)-1-((2S)-3-methyl-2-{[(methyloxy)carbonyl]amino}butanoyl)-2-pyrrolidinyl]-1H-imidazol-4-yl}-4-biphenylyl)-2-oxoethyl]amino}carbonyl)-1,4-dithia-7-azaspiro[4.4]nonane-7-carboxylate (Intermediate 37) (584 mg, 0.71 mmol) and ammonium acetate (546 mg, 7.1 mmol), following the similar procedure outlined in the preparation of Intermediate (22). ES LC-MS m/z=806.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150587B2
Source datasetuspto-grants-2015_10
ORD IDord-b7f8ea4a878347a6bbf23883ef1ed8ee
Source noteuspto-grants-2015_10