Aluminium lithium hydride → 2-{3-[2-(2-Isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-8-yl]-azetidin-1-yl}-2-methyl-propan-1-ol

A solution of 2-{3-[2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-8-yl]-azetidin-1-yl}-2-methyl-propionic acid methyl ester (147 mg, 0.31 mmol) in anhydrous THF (5 mL) at 0° C. under nitrogen was treated dropwise with a 1M solution of LiAlH4 in THF (0.47 mL, 0.47 mmol) and the mixture was stirred for 15 minutes then allowed to warm to RT. After 1.5 hours the mixture was cooled to 0° C. and quenched by cautious addition of water. EtOAc was added and the organic layer was washed with brine, dried (Na2SO4) and concentrated in vacuo. The resultant residue was dissolved in DCM (20 mL) and treated with 4N HCl/dioxan (1 mL). The resulting solid was filtered off, washed with ether and dried to give 427 (142 mg, quant.). LCMS: RT=7.54 min, [M+H]+=440. 1H NMR δ (ppm) (DMSO-d6): 10.61 (1 H, s), 8.32 (1H, d, J=8.21 Hz), 8.07 (1 H, s), 7.22-7.16 (1 H, m), 7.06 (1 H, d, J=1.80 Hz), 5.81-5.72 (1 H, m), 4.55 (1 H, td, J=10.55, 4.79 Hz), 4.38-4.26 (3 H, m), 4.16-3.92 (3 H, m), 3.46-3.37 (5 H, m), 1.53-1.48 (6 H, m), 1.27-1.14 (6 H, m)

1. temperatureAfter 1.5 hours the mixture was cooled to 0° C.
2. customquenched by cautious addition of water
3. additionEtOAc was added
4. washthe organic layer was washed with brine
5. dry with materialdried (Na2SO4)
6. concentrationconcentrated in vacuo
7. dissolutionThe resultant residue was dissolved in DCM (20 mL)
8. additiontreated with 4N HCl/dioxan (1 mL)
9. filtrationThe resulting solid was filtered off
10. washwashed with ether
11. customdried

ORD 기록

ord-5a58d970717349a08a9cd86eda05eb9c

출처 데이터셋

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08952043B2