関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl Ester | HCID 11078219 | — |
| 触媒 | Zincchloride | HCID 3007855 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Nepsilon-dimethylamino-Nalpha-CBZ-O-t-butyl L-lysine | HCID 22883010 | — |
反応手順
A mixture consisting of 3.7 (27.2 mmol) of ZnCl2, 3.2 g (53 mmol) of NaCNBH3 and 60 mL of methanol was prepared to which was added a solution of 18 g (51.7 mmol) of the amine 1 in 180 mL of methanol. After cooling to 10°-15° C. 12.4 mL of 37% formaldehyde (165 mmol) was added dropwise over a 2-3 minute period. The reaction was stirred for 1 hour and monitored by silica gel TLC with elution using a 60:10:1(v/v/v/) mixture of chloroform/methanol/concentrated ammonia (solvent A). One hundred milliliters of water was added and the mixture concentrated to a volume of 200 ml. Ethyl acetate (200 mL) was added and the pH raised to 10.5 with 10% NaOH. The ethyl acetate was separated and the pH of the aqueous phase readjusted to 10.5 and extracted with 200 mL of fresh ethyl acetate. The ethyl acetate extracts were combined, washed with NaCl, dried over Na2SO4, filtered and concentrated to yield, after drying overnight under high vacuum, 14.86 g of viscous oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05723619 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-fcbfd11331bc48daad13c3d9090822ab |
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| 出典メモ | uspto-grants-1998_03 |
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