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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096675Generated: November 3, 2026

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → HCID 123430768, compound

https://huagongshe.com/reaction/1096675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(3S)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]butanoic acidHCID 17040124—
ReactantHCID 66786519HCID 66786519—
Solvent4-MethylmorpholineHCID 7972—
ProductHCID 123430768HCID 123430768—

Reaction Steps

Piperidine (R)-1-(3-methoxypropyl)-2-(piperidin-3-yl)-1H-benzo[d]imidazole (138C) (3.19 g, 11.3 mmol) was acylated with the protected butanoic acid 138B (5 g, 11.4 mmol) in N-methylmorpholine using the standard BOP coupling reaction similar to HATU procedure of Example 7, Step E yielding tert-butyl (S)-2-(9H-fluoren-9-ylamino)-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutylcarbamate (1380) (7.9 g, 11.4 mmol). ESI-MS: m/z 696.6 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138168B1
Source datasetuspto-grants-2012_03
ORD IDord-a2c4c4880f4f4dd8826062aa0599d843
Source noteuspto-grants-2012_03