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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630256Generated: November 1, 2026

(1H-1,2,3-Triazol-1-yl)acetic acid--hydrogen chloride (1/1) → HCID 45257137, compound

https://huagongshe.com/reaction/1630256

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1H-1,2,3-Triazol-1-yl)acetic acid--hydrogen chloride (1/1)HCID 45357676—
ReactantHCID 67010674HCID 67010674—
ProductHCID 45257137HCID 45257137—

Reaction Steps

Proceeding as in Example 1, but substituting 2-(1H-1,2,3-triazol-1-yl)acetic acid hydrochloride and (2S,4R)-4-(2-chloro-4-fluorobenzyl)-N-(4-(4-fluorophenoxy)phenyl)pyrrolidine-2-carboxamide, gave Compound 2, (2S,4R)-1-(2-(1H-1,2,3-triazol-1-yl)acetyl)-4-(2-chloro-4-fluorobenzyl)-N-(4-(4-fluorophenoxy)phenyl)pyrrolidine-2-carboxamide. 1H-NMR (400 MHz, CDCl3): δ 8.96 (s, 1H), 7.79-7.75 (m, 2H), 7.43-7.39 (m, 2H), 7.25-7.13 (m, 2H), 7.03-6.86 (m, 7H), 5.32 (d, 1H), 5.18 (d, 1H), 4.77 (d, 1H), 3.76-3.70 (m, 1H), 3.36 (t, 1H), 3.08-2.96 (m, 1H), 2.94-2.88 (m, 2H), 2.60-2.53 (m, 1H), 1.82-1.73 (m, 1H). MS (EI) for C28H25ClF2N5O3 found 552 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791102B2
Source datasetuspto-grants-2014_07
ORD IDord-aa950995ebb44e9d98c3cd6ffa93434c
Source noteuspto-grants-2014_07