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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223081Generated: November 2, 2026

Acetic Acid → HCID 59713771, compound

https://huagongshe.com/reaction/2223081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2,4,6-Triisopropylbenzenesulfonyl azideHCID 371707—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 59714070HCID 59714070—
ProductHCID 59713771HCID 5971377190.2%

Reaction Steps

As illustrated in the scheme above and following General Procedure 6, KHMDS (10.5 mL of 0.5 M in toluene, 5.25 mmol), 7-chloro-1,3-dihydro-1-methyl-5-(3-pyridinyl)-2H-1,4-benzodiazepin-2-one (1.43 g, 4.99 mmol), trisyl azide (3.86 g, 12.5 mmol) and acetic acid (1.26 mL, 22.0 mmol) were combined. After workup, purification of the crude product by silica gel column chromatography (1:1 CH2Cl2:EtOAc) provided the title compound as a yellow foam (1.47 g, 90%). 1H-NMR (CDCl3): δ 8.80 (s, 1H), 8.76 (d, J=3.6 Hz, 1H), 8.14 (dt, J=1.6 Hz, J=8.0 Hz, 1H), 7.61 (dd, J=2.0 Hz, J=8.4 Hz, 1H), 7.44 (ddd, J=0.8 Hz, J=4.8 Hz, J=8.0 Hz, 1H), 7.38 (d, J=8.8 Hz, 1H), 7.35 (d, J=2.4 Hz, 1H), 4.56 (s, 1H), 3.48 (s, 3H). MS (ESI) (M+H)+=327.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375101B2
Source datasetuspto-grants-2008_05
ORD IDord-8e8a0e2eae1044148776e52e9e738e89
Source noteuspto-grants-2008_05