Hydrochloric Acid → HCID 135518082、化合物
反応式
C[O:2][C:3]1[CH:19]=[CH:18][C:6]2[N:7]=[C:8]([C:10]3[CH:15]=[CH:14][C:13]([O:16]C)=[CH:12][CH:11]=3)[S:9][C:5]=2[CH:4]=1.Cl.N1C=CC=CC=1.Cl>>[OH:16][C:13]1[CH:12]=[CH:11][C:10]([C:8]2[S:9][C:5]3[CH:4]=[C:3]([OH:2])[CH:19]=[CH:18][C:6]=3[N:7]=2)=[CH:15][CH:14]=1参加物
4
実験手順
6-Methoxy-2-(4-methoxy-phenyl)-benzothiazole (134 mg, 0.49 mmol) and pyridine hydrochloride (1.34 g, 11.6 mmol) were heated to 200° C. under nitrogen for 40 min, and then cooled to room temp. Reaction was poured cautiously into aqueous hydrochloric acid (1M) and extracted with ethyl acetate. Ethyl acetate extracts were washed with: 1) hydrochloric acid (1.0M), 2) saturated brine and concentrated in vacuo. Residue was washed with ether/hexane (1:4), dried under vacuum yielding the title compound (119 mg, 100%) as a yellow solid. MH+=244 The starting 6-Methoxy-2-(4-methoxy-phenyl)-benzothiazole was prepared as follows:
後処理
- customReaction
- extractionextracted with ethyl acetate
- washEthyl acetate extracts were washed with: 1) hydrochloric acid (1.0M), 2) saturated brine
- concentrationconcentrated in vacuo
- washResidue was washed with ether/hexane (1:4)
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-e98bcbdd54b24dee92f2a56c1bb7b957
- 出典データセット
- uspto-grants-2006_05
- 特許番号
- US07045539B2
反応ノート
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