Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663575Generated: October 25, 2026

(2S)-2-[2-oxo-4-(1H-tetrazol-1-ylmethyl)-1-pyrrolidinyl]butanamide → HCID 60105793, compound

https://huagongshe.com/reaction/1663575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-[2-oxo-4-(1H-tetrazol-1-ylmethyl)-1-pyrrolidinyl]butanamideHCID 9813710—
Reactant2-[2-oxo-4-(1H-1,2,3-triazol-1-ylmethyl)-1-pyrrolidinyl]butanamideHCID 22387100—
Reactant(2S)-2-[2-oxo-4-(1H-1,2,4-triazol-1-ylmethyl)-1-pyrrolidinyl]butanamideHCID 57478743—
ReactantHCID 57478744HCID 57478744—
Reactant(2S)-2-[2-oxo-4-(4-thiomorpholinylmethyl)-1-pyrrolidinyl]butanamideHCID 66725879—
Reactant(2S)-2-[4-(fluoromethyl)-2-oxo-1-pyrrolidinyl]butanamideHCID 66725939—
Reactant(2S)-2-[2-oxo-4-(1-pyrrolidinylmethyl)-1-pyrrolidinyl]butanamideHCID 66725961—
ProductHCID 60105793HCID 60105793—

Reaction Steps

Alternatively, (2S)-2-[4-(fluoromethyl)-2-oxo-1-pyrrolidinyl]butanamide 44, (2S)-2-[2-oxo-4-(1H-tetrazol-1-ylmethyl)-1-pyrrolidinyl]butanamide 39, (2S)-2-[2-oxo-4-(1H-tetrazol-1-ylmethyl)-1-pyrrolidinyl]butanamide 40, (2S)-2-[2-oxo-4-(1H-1,2,4-triazol-1-ylmethyl)-1-pyrrolidinyl]butanamide 55, 2-[2-oxo-4-(1H-1,2,3-triazol-1-ylmethyl)-1-pyrrolidinyl]butanamide 56, (2S)-2-{4-[(isopropylsulfanyl)methyl]-2-oxo-1-pyrrolidinyl}butanamide 24, (2S)-2-[2-oxo-4-(1-pyrrolidinylmethyl)-1-pyrrolidinyl]butanamide 15, (2S)-2-[2-oxo-4-(4-thiomorpholinylmethyl)-1-pyrrolidinyl]butanamide 17, are prepared in similar ways, from activated alcohol derivatives, such as mesylates, tosylates or halides.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034958B2
Source datasetuspto-grants-2011_10
ORD IDord-b2afd32a152e4a9f9af37bc75b21c0fa
Source noteuspto-grants-2011_10