참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | 4-Amino-1-butanol | HCID 25868 | — |
| 반응물 | N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanine | HCID 6992569 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Boc-Ala-Ala-NH-(CH2)4-OH | HCID 59537080 | 75% |
반응 단계
To a vigorously stirring solution of Boc-(Ala)2-OH (0.9 gm, 3.46 mmol) and NMM (0.57 mL, 5.2 mmol) in THF (20 mL) cooled to −15° C. was added under N2 atmosphere ethyl chloroformate (ECF) (372 μL, 3.56 mmol) and stirred for 2 min. A solution of H2N(CH2)4OH (462 mg, 5.19 mmol) in THF (5 mL) was added to the mixture followed by NMM (950 μL, 8.65 mmol) and the mixture was warmed to r.t. and stirred until silica gel TLC indicated complete consumption of the starting acid (eluting solvent—MeOH:DCM—1:10, Rf—0.45) (˜8 h). The solvent was evaporated, and the residue was diluted with EtOAc and washed with brine, water, saturated solutions of citric acid and NaHCO3, and the organic layer was dried using NaHSO4, and the solvent was removed under vacuum to yield a residue which was purified using silica gel flash column chromatography—Hexanes:EtOAc—1:3; to give the desired product in 75% yield (858 mg) as a solid—m.p.—102-104° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08563686B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-bd9d8cd11099458aa2f8c3dce2987f7f |
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| 출처 메모 | uspto-grants-2013_10 |
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