関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | [2-(5-Methyl-sulfanyl-2-nitro-phenylamino)-ethyl]-carbamic acid tert-butyl ester | HCID 86615412 | — |
| 触媒 | Nickel Dichloride | HCID 24385 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | [2-(2-amino-5-Methyl-sulfanyl-phenylamino)-ethyl]-carbamic acid tert-butyl ester | HCID 86615411 | — |
反応手順
In a 500 mL round bottom flash equipped with a stir bar was charged with MeOH (200 mL), [2-(5-methyl-sulfanyl-2-nitro-phenylamino)-ethyl]-carbamic acid tert-butyl ester (5 g, 0.02 mol) and NiCl2 (19 g, 0.05 mol) and cooled to 0° C. NaBH4 (1.7 g, 0.05 mol) was added (in four equal portions) to the reaction mixture over a 1 h period. Once the addition was complete the reaction mixture was stirred for an additional 2 h. Brine (100 mL) and ethyl acetate (200 mL) were added to the reaction mixture. The heterogeneous mixture was transferred to a separatory funnel where the aqueous phase was separated and re-extracted with ethyl acetate (2×100 mL). The organic phases were combined and washed with H2O (3×100 mL), brine (100 mL), dried over MgSO4, filtered and concentrated under reduced pressure to give a black residue. The crude product was dissolved in 100 mL of CH2Cl2 and separated into two 100 mL round (50 mL in each) and both were concentrated under reduced pressure and used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07741355B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-db976b0046da4a7a84077472e892d2a8 |
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| 出典メモ | uspto-grants-2010_06 |
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