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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541632Generated: November 1, 2026

Pivaloyl chloride → HCID 69014469, compound

https://huagongshe.com/reaction/541632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 86636141HCID 86636141—
ProductHCID 69014469HCID 6901446931%

Reaction Steps

The desired compound was prepared according to the procedure of Example A20, using N-[6-chloro-2,4,8,22-tetraazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-piperidin-4-ylacetamide bis(trifluoroacetate) and 2,2-dimethylpropanoyl chloride as starting materials in 31% yield. 1H NMR (300 MHz, DMSO-d6): δ 9.50 (s, 1H), 9.33 (s, 1H), 9.30 (s, 1H), 8.13 (s, 1H), 7.98 (s, 1H), 7.77 (s, 1H), 7.21 (d, 1H), 7.04 (m, 2H), 6.87 (d, 1H), 6.79 (d, 1H), 4.27 (m, 2H), 2.81 (m, 6H), 2.25 (m, 2H), 2.01 (m, 1H), 1.76 (m, 2H), 1.19 (s, 9H), 1.04 (m, 2H). LCMS for C30H36ClN6O2 (M+H)+: m/z=547.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-01acf1e7c33141de98007cca789a94fe
Source noteuspto-grants-2014_10