Phosphorus oxychloride → 2-Methyl-5-(2-nitro-phenylamino)-thiazole-4-carbonitrile

HRID 1350443Notes

Reaction equation

[CH3:1][C:2]1[S:3][C:4]([NH:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[N+:17]([O-:19])=[O:18])=[C:5]([C:7]([NH2:9])=O)[N:6]=1.O=P(Cl)(Cl)Cl>C1(C)C=CC=CC=1>[CH3:1][C:2]1[S:3][C:4]([NH:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[N+:17]([O-:19])=[O:18])=[C:5]([C:7]#[N:9])[N:6]=1

Participants

Conditions

Temperature: 0 °C

Procedure

Combine 2-methyl-5-(2-nitroanilino)thiazole-4-carboxylic acid amide (60 g, 215 mmol) and toluene and add POCl3 (40 mL, 430 mmol) and reflux the reaction mixture. After 2.5 h cool to 0° C. Add saturated NaHCO3 solution to quench the extra POCl3 (Caution!!) until the aqueous was around pH 8. Add ethyl acetate (2×2 L) to extract the product. Combined organic layer and wash with brine (2×1 L), dry over MgSO4, and evaporate to give a reddish solid which triturated with 25% ethyl acetate in hexane to give a reddish solid (36 g). Evaporate the filtrate to half volume to give second batch of compound (3.2 g). Total yield (39.2 g, 70%): mass spectrum (m/e): 261 (M+1); 1HNMR(300 MHz, DMSO, ppm): 2.70 (s, 1H), 7.02 (t, 1H), 7.22 (d, 1H), 7.58 (t, 1H), 8.25 (d, 1H), 9.78 (s, 1H). ). 13CNMR(75MHz, DMSO, ppm): 20.4, 113.1, 116.2, 118.7, 121.2 127.0, 134.9, 136.6, 140.0, 148.6, 161.5. Formula: C11H8N4O2S

Workup

temperaturereflux the reaction mixture
customAdd saturated NaHCO3 solution to quench the extra POCl3 (Caution!!) until the
extractionAdd ethyl acetate (2×2 L) to extract the product
washCombined organic layer and wash with brine (2×1 L)
dry with materialdry over MgSO4
customevaporate
customto give a reddish solid which
customtriturated with 25% ethyl acetate in hexane

Sources & evidence

ORD record: ord-0009f3c47a9743f2996e2249dc6ecd2b
Source dataset: uspto-grants-2007_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07214673B2

Reaction notes

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