반응 #661492

ord-ead88de655fe4d0a85071c38f67f0a28

반응 방정식

CCCN(CCN1CCNCC1)C1CCc2c(O)cccc2C1
39b
CCCN(CCN1CCNCC1)C1CCc2c(O)cccc2C1
6-[(2-Piperazin-1-yl-ethyl)-propyl-amino]-5,6,7,8-tetrahydro-naphthalen-1-ol
O=C(O)c1cc2ccccc2s1
benzo[b]thiophene-2-carboxylic acid
CCCN(CCN1CCN(C(=O)c2cc3ccccc3s2)CC1)C1CCc2c(O)cccc2C1
40i
수율 99.9%
CCCN(CCN1CCN(C(=O)c2cc3ccccc3s2)CC1)C1CCc2c(O)cccc2C1
Benzo[b]thiophen-2-yl-(4-{2-[(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-ethyl}-piperazin-1-yl)-methanone
수율 99.9%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Compound 40i was prepared

실험 절차

Compound 40i was prepared following Procedure G using 39b (175 mg, 0.551 mmol) and benzo[b]thiophene-2-carboxylic acid (118 mg, 0.661 mmol) to give 40i (263 mg, 64%) after column chromatography. 1H NMR (400 MHz, CD3OD) 0.91-0.97 (t, 3H, J=7.2 Hz), 1.53-1.68 (m, 3H), 2.50-2.63 (m, 7H), 2.78-3.02 (m, 7H), 3.77-3.79 (bs, 4H), 6.55-6.59 (t, 2H, J=8 Hz), 6.89-6.93 (t, 1H, J=8.4 Hz), 7.40-7.46 (m, 2H), 7.61 (s, 1H), 7.85-7.91 (m, 2H). The free base of 40i was converted into its HCl salt. m.p. 131-134° C. Anal. [C28H35N3O2S.2HCl.1.5H2O] C, H, N.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09034877B2uspto-grants-2015_05