Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetone → (1S,9aS) N-[(7-Azidoacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo [3,4-a]indol-1-yl)methyl]acetamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Sodium Azide | HCID 33557 | — |
| 반응물 | (1S,9aS) N-[(7-Chloroacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamide | HCID 18653087 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Dichloromethane methanol | HCID 21226129 | — |
| 용매 | Ethylacetate methanol | HCID 21584119 | — |
| 생성물 | (1S,9aS) N-[(7-Azidoacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo [3,4-a]indol-1-yl)methyl]acetamide | HCID 86747041 | — |
반응 단계
A mixture of (1S,9aS) N-[(7-chloroacetyl-9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamide (EXAMPLE 48, 43 mg) and sodium azide (82 mg) are stirred in aqueous tetrahydrofuran (66%) for 3 days. Acetone (1 ml) is added and the mixture was heated in an oil bath (38°-50°) for 8 hours then concentrated to an aqueous layer and extracted with ethylacetate (6×2 ml). The combined organic layers are dried over magnesium sulfate and concentrated to provide the product as as an oil. The oil is taken up in methylene chloride/methanol and then placed on a 100 μsilica preprative plate and developed in methanol/ethylacetate (10/90, 2×) to give the title compound. ##STR2##
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05247090 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-344b5d26f989476db51adec38886cea4 |
| 출처 메모 | uspto-grants-1993_09 |