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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437578Generated: November 2, 2026

Acetic Anhydride → HCID 16736941, compound

https://huagongshe.com/reaction/1437578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDanegaptideHCID 16656685—
SolventFormic AcidHCID 284—
ProductHCID 16736941HCID 1673694129%

Reaction Steps

Acetic anhydride (Acros) (0.32 mL, 3.4 mmol, 10 equivalents) was added dropwise to a solution of (2S,4R) 1-(2-Amino-acetyl)-4-benzoylamino-pyrrolidine-2-carboxylic acid (Compound 2, 0.1 g, 0.34 mmol, 1 equivalent) in formic acid (J. T. Baker) (1 mL) at 0° C. After the addition was complete, the reaction mixture was allowed to warm to room temperature and stirred an additional 24 hours. The reaction mixture was monitored by TLC and LCMS. An additional amount of acetic anhydride (0.32 mL, 3.4 mmol, 10 equivalents) was added and the reaction mixture stirred for 24 hours at room temperature. Ice-water (1 mL) was added and the volatiles were removed in vacuo to yield an oily crude product that was further purified by HPLC (column:Waters Atlantis 19×150 mm) using 0.1% formic acid in H20/MeOH 20-40% MeOH over 15 minute gradient to afford 0.031 g (29%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622496B2
Source datasetuspto-grants-2009_11
ORD IDord-26a8bc78bcfe4e29b9932a303ff2e162
Source noteuspto-grants-2009_11