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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816927Generated: November 3, 2026

5-Bromo-4-methylthiophene-2-carbonitrile → HCID 11292353, compound

https://huagongshe.com/reaction/1816927

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-4-methylthiophene-2-carbonitrileHCID 21986234—
ReactantHCID 68863777HCID 68863777—
ProductHCID 11292353HCID 11292353—

Reaction Steps

Prepared from 7-bromo-5-ethyl-5-thien-2-yl-1,5-dihydro-4,1-benzoxazepin-2(3H)-one and 5-bromo-4-methyl-thiophene-2-carbonitrile generally according to the procedures described in examples 82 and 1. An off-white solid: mp 182-184° C.; 1H NMR (DMSO-d6): δ 10.19 (s, 1H), 7.83 (s, 1H), 7.57 (dd, J=4.88, 0.98 Hz, 1H), 7.46 (dd, J=8.3, 1.95 Hz, 1H), 7.33 (d, J=1.95 Hz, 1H), 7.29 (d, J=8.3 Hz, 1H), 7.07 (dd, J=4.88, 3.42 Hz, 1H), 6.98 (dd, J=3.42, 0.98 Hz, 1H), 4.14 (d, J=15.6 Hz, 1H), 3.98 (d, J=15.13 Hz, 1H), 2.47 (m, 1H), 2.35 (m, 1H), 2.21 (s, 3H), 0.77 (t, J=6.84 Hz, 3H); MS (ESI) m/z 395 ([M+H]+); MS (ESI) m/z 393 ([M−H]−); Anal. calcd for C21H18N2O2S2: C, 63.93; H, 4.60; N, 7.10. Found: C, 60.33; H, 4.13; N, 6.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598237B2
Source datasetuspto-grants-2009_10
ORD IDord-a84fe575210348b7a76007431083bc2a
Source noteuspto-grants-2009_10