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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570508Generated: October 30, 2026

1-BOC-3-Aminopiperidine → HCID 66958099, compound

https://huagongshe.com/reaction/570508

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BOC-3-AminopiperidineHCID 545809—
Reactant3-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-thiophene-2-carboxylic acid benzylamideHCID 50923861—
ProductHCID 66958099HCID 6695809914%

Reaction Steps

The title compound was prepared in an analogous manner as 3-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-thiophene-2-carboxylic acid benzylamide using tert-butyl 3-aminopiperidine-1-carboxylate instead of benzylamine and obtained in 14% yield. 1H NMR (DMSO-d6) 11.96 (br s, 1H), 11.39 (br s, 1H), 8.47 (d, J=5.8 Hz, 1H), 8.38 (s, 1H), 8.09-8.01 (m, 1H), 7.78 (d, J=4.8 Hz, 1H), 7.38-7.14 (m, 1H), 6.48-6.43 (m, 1H), 3.91-3.75 (m, 3H), 2.80-2.62 (m, 3H), 1.92-1.84 (m, 1H), 1.75-1.66 (m, 1H), 1.65-1.54 (m, 1H), 1.40 (s, 9H); MS (m/z) 443 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023847B2
Source datasetuspto-grants-2015_05
ORD IDord-8e26ff6c492e46c691a0826be82fd27b
Source noteuspto-grants-2015_05