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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039745Generated: October 30, 2026

m-Aminoacetanilide → HCID 58327720, compound

https://huagongshe.com/reaction/2039745

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-AminoacetanilideHCID 7604—
ReactantHCID 86654847HCID 86654847—
ProductHCID 58327720HCID 58327720—

Reaction Steps

N-(3-((5-(2-Methylbenzo yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)phenyl)acetamide was synthesized using N-(3-aminophenyl)acetamide and ((4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)(o-tolyl)methanone according to the general procedure A. An off-white solid was obtained. M.p.>300° C.; 400 MHz 1HNMR (DMSO-d6) δ 11.36 (s, 1H), 10.01 (s, 1H), 8.46 (s, 1H), 8.06 (s, 1H), 7.73 (d, J=7.6 Hz, 1H), 7.57 (s, 1H), 7.49-7.45 (m, 2H), 7.39-7.28 (m, 4H), 2.34 (s, 3H), 2.02 (s, 3H); LCMS [M+H] 386.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580803B2
Source datasetuspto-grants-2013_11
ORD IDord-707d73c5754d43c69fb715818cc6cf69
Source noteuspto-grants-2013_11