反応式
[S:1]1[C:5]2[CH:6]=[C:7]([NH:10][CH2:11][CH:12]([CH3:16])C(O)=O)[CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.C([N:19]([CH2:22]C)CC)C.C1C=CC(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:31])=CC=1.C1(C)C=CC=CC=1>C(Cl)(Cl)Cl.CO>[S:1]1[C:5]2[CH:6]=[C:7]([N:10]3[CH2:11][CH:12]([CH3:16])[NH:19][C:22]3=[O:31])[CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1参加物
7
実験手順
3-(Benzothiazol-6-ylamino)-2-methyl-propionic acid (I-167a: 500 mg, 2.118 mmol) was refluxed with triethylamine (1 mL, 6.989 mmol), DPPA (1.75 g, 6.35 mmol) and toluene (10 mL) at 120° C. in a sealed tube to afford the crude product. The reaction was monitored by TLC (5% methanol in chloroform). Purification by column chromatography on silica gel (2% methanol in chloroform) afforded 350 mg of the product (71.42% yield).
後処理
- customto afford the crude product
- customPurification by column chromatography on silica gel (2% methanol in chloroform)
出典と根拠
- ORDレコード
- ord-16977979bb3b4bca80d592a1b71ee22b
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08263635B2
関連ノート
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