Sodium Hydroxide → Tert-butyl{2-[({5-[(chloroacetyl)amino]-benzothien-2-yl}carbonyl)amino]-phenyl}carbamate
反応式
[Cl:1][CH2:2][C:3]([NH:5][C:6]1[CH:7]=[CH:8][C:9]2[S:13][C:12]([C:14]([O:16]C)=O)=[CH:11][C:10]=2[CH:18]=1)=[O:4].[OH-:19].[Na+].ClCC(NC1C=C[C:29]2SC(C(O)=O)=[CH:31][C:30]=2[CH:37]=1)=O.CCN=C=NCCCN(C)C.[CH:49]1[CH:50]=[CH:51][C:52]2[N:57](O)N=[N:55][C:53]=2[CH:54]=1.C1[CH2:63][O:62]CC1.CO>CN(C=O)C.C(Cl)Cl>[C:30]([O:19][C:63](=[O:62])[NH:55][C:53]1[CH:54]=[CH:49][CH:50]=[CH:51][C:52]=1[NH:57][C:14]([C:12]1[S:13][C:9]2[CH:8]=[CH:7][C:6]([NH:5][C:3](=[O:4])[CH2:2][Cl:1])=[CH:18][C:10]=2[CH:11]=1)=[O:16])([CH3:29])([CH3:31])[CH3:37]参加物
反応物 6
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of methyl 5-[(chloroacetyl)amino]-1-benzothiophene-2-carboxylate (1.26 g, 4.50 mmol) in THF/MeOH (16/16 μL) was added 2N NaOH (9 mL). After 4 h, the solvent was reduced and the aqueous was washed with EtOAc. The aqueous was acidified and the solids were filtered and used without further purification. To a solution of 5-[(chloroacetyl)amino]-1-benzothiophene-2-carboxylic acid (765 mg, 2.84 mmol) in DMF (3 mL) and CH2Cl2 (10 mL) was added EDCI (652 mg, 3.4 mmol), HOBt (460 mg, 3.40 mmol). The reaction mixture was stirred for 20 min and Boc-protected phenylene diamine (650 g, 3.12 mmol) was added. After 18 h, the solvent was removed and the residue was triturated with EtOAc and H2O. The solids were and filtered yielding the desired product as a solid, which was used without further purification. MS: cal'd 460 (MH+), exp 460 (MH+).
後処理
- washthe aqueous was washed with EtOAc
- filtrationthe solids were filtered
- customused without further purification
- additionBoc-protected phenylene diamine (650 g, 3.12 mmol) was added
- waitAfter 18 h
- customthe solvent was removed
- customthe residue was triturated with EtOAc and H2O
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-aa8ff8a5a80a48b882f53c28f00cd23b
- 出典データセット
- uspto-grants-2010_11
- 特許番号
- US07834034B2
反応ノート
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