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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039747Generated: October 30, 2026

3-Amino-N-methylbenzamide → HCID 58327745, compound

https://huagongshe.com/reaction/2039747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-N-methylbenzamideHCID 676526—
ReactantHCID 86654848HCID 86654848—
ProductHCID 58327745HCID 58327745—

Reaction Steps

3-((5-(1-Naphthoyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-methylbenzamide was synthesized using 3-amino-N-methylbenzamide and (4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)(naphthalen-1-yl)methanone according to the general procedure A. A yellow solid was obtained. M.p.>300° C.; 400 MHz 1HNMR (DMSO-d6) δ 11.53 (s, 1H), 8.48-8.44 (m, 2H), 8.24-8.20 (m, 2H), 8.14 (d, J=8.0 Hz, 1H), 8.06-8.03 (m, 2H), 7.80-7.78 (m, 1H), 7.70 (d, J=2.4 Hz, 1H), 7.64-7.53 (m, 3H), 7.50-7.44 (m, 2H), 2.77 (d, J=4.4 Hz, 3H); LCMS [M+H] 422.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580803B2
Source datasetuspto-grants-2013_11
ORD IDord-ebe3def36cb9470988a412e0a1433db3
Source noteuspto-grants-2013_11